Buy Dolethal 100ml Solution For Injection Online
Dolethal 100ml is a veterinary injectable product containing pentobarbital sodium, a barbiturate used in veterinary medicine for euthanasia. Current official veterinary medicine records identify Dolethal at 200 mg/ml pentobarbital sodium, with a 100 ml vial presentation authorized in certain markets. The exact presentation, target species, and dispensing requirements can vary by country, so product information should always be checked against the applicable local authorization.
For World Equine Vet, Dolethal 100ml should be presented as a professionally regulated veterinary medicine rather than as an ordinary animal-health product. It is subject to veterinary prescription requirements in markets such as the UK and Ireland, and official records identify pentobarbital-containing veterinary medicines as controlled or specially regulated products in several jurisdictions.
Important: Dolethal contains pentobarbital sodium and is intended for veterinary use by appropriately authorized professionals. This page provides product and regulatory information only and does not provide euthanasia dosing or administration instructions.
What Is Dolethal 100ml?
Dolethal 100ml is a solution for injection containing pentobarbital sodium. Official veterinary medicine databases identify the Dolethal formulation at 200 mg of pentobarbital sodium per ml. A 100 ml vial therefore represents the 100 ml package presentation of this veterinary medicine, rather than a different concentration.
Dolethal is manufactured by Vetoquinol, a veterinary pharmaceutical company, and is authorized in a number of European markets under different national or regional regulatory frameworks. Current records show Dolethal 200 mg/ml authorized for dogs and cats in Ireland and the Netherlands, while the UK product information identifies Dolethal 200 mg/ml as a prescription veterinary medicine and includes a 100 ml presentation.
The product’s principal veterinary purpose is euthanasia. The UK Summary of Product Characteristics identifies Dolethal 200 mg/ml for euthanasia of small animals, mainly dogs and cats, and cattle. Other national authorizations can specify different target species or presentations, making jurisdiction-specific verification important before discussing the product for a particular animal.
Because pentobarbital is a potent barbiturate and regulated substance, Dolethal should not be treated like a general-purpose injectable veterinary supplement or routine over-the-counter animal-health product.
Dolethal 100ml Overview
Product characteristic Information Product name Dolethal 100ml Product type Veterinary solution for injection Active substance Pentobarbital sodium Concentration 200 mg/ml Package presentation 100 ml vial in markets where this presentation is authorized Manufacturer / marketing authorization holder Vetoquinol Primary veterinary purpose Euthanasia Administration Veterinary professional use according to the applicable product authorization Prescription status Veterinary prescription requirements apply in relevant markets Regulatory classification Regulated veterinary medicine; controlled-drug requirements may apply depending on jurisdiction The official European veterinary medicines database lists Dolethal 200 mg/ml as a solution for injection containing pentobarbital sodium and identifies veterinary prescription status in Ireland. The UK regulatory information likewise identifies Dolethal as a prescription veterinary medicine.
Active Ingredient: Pentobarbital Sodium
The active substance in Dolethal is pentobarbital sodium.
The current UK product information specifies 200.00 mg of pentobarbital sodium per ml. It also identifies benzyl alcohol and Ponceau 4R among the other constituents.
Pentobarbital belongs to the barbiturate class of medicines. In veterinary euthanasia products, its pharmacological action is intended to produce profound central nervous system depression leading to loss of consciousness followed by cessation of vital functions when administered appropriately by a veterinary professional.
Because of its pharmacological potency, pentobarbital is not suitable for casual, unsupervised, or experimental use.
Why the Active Ingredient Matters
When researching Dolethal 100ml, buyers should verify:
- The active substance
- The concentration
- The vial size
- The manufacturer
- The target species listed on the applicable label
- The country of authorization
- The prescription classification
- The product’s expiry information
- The batch or lot information
- The applicable storage requirements
These details are especially important with veterinary medicines containing controlled substances.
Product Form and Presentation
Dolethal is supplied as a solution for injection. Current UK documentation describes the product as a pink liquid solution, while the European Union veterinary medicine database describes the 100 ml presentation as a Type II glass vial containing a red aqueous solution closed with a rubber stopper and aluminium cap.
The 100 ml presentation is specifically documented in current Irish and UK product information. The Irish authorization lists both 100 ml and 50 ml glass vial presentations, while the current UK product documentation identifies 100 ml and 250 ml presentations.
This demonstrates why product pages should not assume that every Dolethal presentation is available in every country.
For example, the current French authorization information lists different authorized presentations, while the Netherlands database identifies Dolethal 200 mg/ml for dogs and cats but does not present the same package information as the Irish record.
Veterinary Use of Dolethal 100ml
Dolethal is a veterinary euthanasia product.
The current UK Summary of Product Characteristics states that Dolethal 200 mg/ml is indicated for euthanasia of small animals, mainly dogs and cats, and cattle. Other national product records may have narrower target-species descriptions; for example, the current Irish and Dutch records identify dogs and cats.
This distinction is important for an international website.
A product may have different authorized species, presentations, routes, or legal classifications depending on the market in which it is registered. World Equine Vet should therefore avoid presenting one country’s product authorization as universally applicable.
Professional Veterinary Context
Dolethal is intended for use within an appropriate veterinary setting and under the authority of an appropriately qualified professional.
The product should be selected and used according to:
- The applicable veterinary medicine authorization
- Local prescription requirements
- The veterinarian’s professional judgment
- The species and circumstances identified in the authorization
- Applicable controlled-drug requirements
- Appropriate handling and disposal procedures
World Equine Vet should not present Dolethal as a product for unsupervised administration.
Dolethal 100ml for Veterinary Professionals
Veterinary professionals researching Dolethal 100ml may be interested in several practical product characteristics.
Formulation
The currently documented Dolethal formulation contains 200 mg/ml pentobarbital sodium.
Package Size
The 100 ml vial is an authorized presentation in some markets, including the current Irish and UK documentation.
Manufacturer
Current official records identify Vetoquinol as the marketing authorization holder/manufacturer associated with Dolethal in the relevant markets.
Product Status
Dolethal is not a general retail animal-health product. Current regulatory sources identify it as a prescription veterinary medicine, while UK government information places Dolethal among authorized veterinary medicines containing controlled drugs.
Key Features of Dolethal 100ml
Important characteristics include:
- 200 mg/ml pentobarbital sodium
- Injectable veterinary formulation
- 100 ml vial presentation in applicable markets
- Manufactured/marketed by Vetoquinol
- Intended for veterinary euthanasia
- Regulated veterinary medicine
- Prescription requirements in applicable jurisdictions
- Professional veterinary administration
- Country-specific authorization and labeling
- Controlled-drug considerations in relevant jurisdictions
The precise legal status and authorized use should always be determined from the current product information applicable to the destination country.
Benefits and Important Considerations
When evaluating Dolethal 100ml as a veterinary product, the most important consideration is not simply package size. Veterinary professionals should also verify that the product is the correct authorized formulation for the intended use and jurisdiction.
Product consistency
The 200 mg/ml formulation provides a clearly specified concentration, allowing veterinary professionals to identify the product accurately from its packaging and regulatory documentation.
Established veterinary product
Dolethal has a long history of veterinary authorization. The Irish regulatory record identifies a marketing authorization date of 1990, while the French record identifies authorization dating to 1992.
Professional-use positioning
Dolethal’s regulatory status reinforces that it is a professional veterinary medicine rather than a consumer animal-care product.
Important limitation
Availability and authorized presentation are not universal. A Dolethal 100ml vial listed in one country should not automatically be assumed to be legally marketed or available in another.
Veterinary and Equine Considerations
Despite the World Equine Vet brand name, the currently reviewed Dolethal 200 mg/ml authorizations do not establish the product as a general equine medicine.
The Irish and Dutch records identify dogs and cats as target species, while the UK product information identifies small animals and cattle. Therefore, the page should not imply that the Dolethal 200 mg/ml 100 ml presentation is universally authorized for horses.
This is an important distinction for an equine-focused website.
Where a veterinary professional is considering a pentobarbital-containing euthanasia product for a horse or another species, the applicable local veterinary authorization should be checked rather than assuming that the authorization for dogs, cats, or cattle applies to horses.
Important Safety Information
Dolethal contains pentobarbital sodium, a potent barbiturate. It should be handled only by appropriately authorized veterinary professionals.
The official product information warns that intravenous pentobarbital can cause induction excitement in some animals and states that appropriate sedation should be used where the veterinarian considers it necessary. The product information also emphasizes avoiding administration outside the intended vascular route because this can reduce effectiveness.
Because the administration of euthanasia medicines involves significant veterinary and welfare considerations, this product page intentionally does not provide a dosing protocol or step-by-step administration instructions.
Important precautions
Professional users should consult the current approved product information for:
- Contraindications
- Species-specific requirements
- Administration requirements
- Sedation considerations
- Adverse reactions
- Drug interactions
- Disposal requirements
- Controlled-drug requirements
The applicable label and professional veterinary judgment should take precedence over general online product information.
Contraindications and Restrictions
The current UK Dolethal product information states that the medicine should not be used in animals intended for animal consumption and should not be used for anaesthesia.
The exact contraindications and warnings can vary with the authorized formulation and jurisdiction, so veterinary professionals should consult the current national product information rather than relying on a generalized online description.
Prescription and Controlled-Drug Considerations
Dolethal requires particular attention to regulatory compliance.
The European veterinary medicines database identifies Dolethal 200 mg/ml as a veterinary medicinal product subject to veterinary prescription in Ireland. The Dutch database classifies the product as UDD, meaning it is restricted to veterinary use under the applicable Dutch framework.
UK government information also lists Dolethal 200 mg/ml among authorized veterinary medicines containing Schedule 3 controlled drugs, with pentobarbital sodium identified as the active substance.
Canada’s product database previously listed Dolethal 200 mg/ml as a controlled veterinary drug, although that particular Canadian authorization is currently shown as cancelled.
International purchasing
International customers should not assume that a prescription or authorization from one country automatically permits the purchase, importation, possession, or use of Dolethal in another.
Importation and distribution of controlled veterinary medicines can be subject to additional requirements.
Storage and Handling
Storage requirements should be taken from the current product label and the applicable national product information.
Veterinary professionals should pay particular attention to:
- The manufacturer’s storage temperature requirements
- Protection from inappropriate environmental conditions
- Expiry date
- Container integrity
- Batch or lot identification
- Controlled-drug storage requirements
- Disposal of unused product
- National requirements for veterinary pharmaceutical waste
The current UK product information also states that unused Dolethal must be destroyed in accordance with applicable controlled-drug requirements and should not be disposed of through wastewater.
After opening
The post-opening shelf life can be jurisdiction-specific. The current UK product information reports a defined shelf life after first opening, so veterinary professionals should follow the current label for the particular market and product supplied rather than applying a generic assumption.
Packaging and Product Verification
When receiving Dolethal 100ml, professional purchasers should check the packaging carefully.
Useful verification points include:
- Product name
- Active substance
- Concentration
- Package size
- Manufacturer
- Marketing authorization information
- Batch number
- Expiry date
- Packaging integrity
- Applicable regulatory labeling
For a product containing a controlled substance, maintaining appropriate purchasing and inventory records is particularly important.
How to Identify Dolethal 100ml
A current authorized 100 ml Dolethal presentation can be identified by its product name, concentration, manufacturer information, and vial size.
The current UK documentation identifies Dolethal 200 mg/ml Solution for Injection and lists a 100 ml vial presentation. The Irish authorization likewise identifies a 100 ml Type II glass vial.
Because package presentations differ between markets, buyers should compare the physical product with the regulatory documentation applicable to their country.
Dolethal 100ml vs. Other Pentobarbital Veterinary Products
Dolethal is one of several veterinary medicines containing pentobarbital sodium.
Other products listed in current UK government information include Euthanimal 20% at 200 mg/ml, Euthanimal 40% at 400 mg/ml, Euthasol Vet at 400 mg/ml, and Euthoxin at 500 mg/ml.
This comparison demonstrates why the concentration should never be inferred simply from the fact that a product contains pentobarbital.
For example:
Product Documented concentration Dolethal 200 mg/ml Euthanimal 20% 200 mg/ml Euthanimal 40% 400 mg/ml Euthasol Vet 400 mg/ml Euthoxin 500 mg/ml These products should not be considered interchangeable simply because they contain the same active substance. Their authorized species, formulation, concentration, labeling, and legal requirements may differ.
Purchasing Considerations
When sourcing Dolethal 100ml, professional buyers should prioritize legitimate veterinary pharmaceutical supply channels.
Important considerations include:
Authorized supply
Purchase should be through a supplier legally authorized to distribute veterinary prescription medicines in the relevant jurisdiction.
Prescription requirements
Where Dolethal is classified as a prescription veterinary medicine, the appropriate prescription or professional authorization should be obtained before supply.
Product authenticity
The packaging should contain appropriate manufacturer and regulatory information, including batch and expiry details.
Correct concentration
Dolethal 200 mg/ml should not be confused with other pentobarbital products at higher concentrations.
Country-specific legality
The legal availability of a product can differ substantially between countries. A product authorized in one market may not have the same authorization elsewhere.
Shipping and Availability
Shipping of Dolethal 100ml requires more consideration than ordinary veterinary products because pentobarbital is regulated.
Professional purchasers should verify:
- Whether the product can legally be supplied to the destination
- Whether a prescription is required
- Whether the recipient is legally entitled to receive it
- Whether controlled-drug transport rules apply
- Whether import authorization is required
- Whether the carrier accepts the shipment
- Whether local veterinary pharmaceutical regulations impose additional requirements
World Equine Vet should not advertise guaranteed international delivery of Dolethal or imply that regulatory requirements can be bypassed.
Availability can also vary because different national markets authorize different presentations.
Where To Buy Dolethal 100ml Online
Dolethal 100ml should be sourced only through a legitimate, appropriately authorized veterinary pharmaceutical supplier or veterinary practice where the product is legally available.
The current official regulatory information identifies Dolethal 200 mg/ml as a prescription veterinary medicine in relevant markets.
For customers considering Dolethal 100ml, the most important purchasing checks are:
- Confirm that Dolethal is authorized in your country.
- Confirm that the 100 ml presentation is legally marketed in that jurisdiction.
- Obtain any required veterinary prescription or professional authorization.
- Verify the concentration as 200 mg/ml for the Dolethal formulation discussed on this page.
- Confirm the manufacturer and product labeling.
- Check the batch and expiry information upon receipt.
- Follow all applicable controlled-drug requirements.
- Use the product only within the professional veterinary framework established by the applicable authorization.
Because Dolethal contains pentobarbital sodium, World Equine Vet should not position the product as an unrestricted consumer purchase or promote methods of obtaining it without the required veterinary authorization.
Why Choose a Professional Veterinary Supplier?
A professional veterinary supplier can provide greater transparency around:
- Product identity
- Manufacturer
- Regulatory authorization
- Package size
- Batch information
- Expiry information
- Prescription requirements
- Shipping restrictions
- Storage requirements
- Appropriate documentation
This is particularly important for regulated veterinary medicines.
A professional purchasing process also helps reduce the risk of receiving an incorrectly labeled, expired, improperly stored, or unauthorized product.
Frequently Asked Questions
What is Dolethal 100ml?
Dolethal 100ml is a 100 ml presentation of Dolethal veterinary solution for injection containing pentobarbital sodium. Current official product information identifies the Dolethal formulation discussed here as 200 mg/ml.
What is the active ingredient in Dolethal?
The active ingredient is pentobarbital sodium. The current Dolethal 200 mg/ml formulation contains 200 mg of pentobarbital sodium per ml.
What is Dolethal used for?
Dolethal is a veterinary medicine used for euthanasia. The precise authorized target species depend on the national authorization. Current UK information identifies small animals, mainly dogs and cats, and cattle, while other national records identify dogs and cats.
Is Dolethal 100ml a prescription veterinary medicine?
Yes. Current official veterinary medicine information identifies Dolethal as subject to veterinary prescription requirements in relevant markets.
Is Dolethal a controlled drug?
Pentobarbital-containing veterinary medicines are subject to controlled-drug regulations in some jurisdictions. For example, UK government information lists Dolethal 200 mg/ml among authorized veterinary medicines containing controlled drugs.
Is Dolethal 100ml available in every country?
No. Package sizes, target species, marketing authorization, and supply status can differ between countries. The current Irish and UK records document a 100 ml presentation, while other national records show different presentation information.
Is Dolethal 200 mg/ml the same as every pentobarbital injection?
No. Other veterinary pentobarbital products are available in different concentrations, including 400 mg/ml and 500 mg/ml products. They should not be assumed to be interchangeable.
Can Dolethal be used as an anaesthetic?
The current UK product information specifically states that Dolethal should not be used for anaesthesia.
Can Dolethal be used in animals intended for human consumption?
The current UK product information states that Dolethal should not be used in animals intended for animal consumption.
Does World Equine Vet recommend administering Dolethal without a veterinarian?
No. Dolethal is a regulated veterinary medicine containing pentobarbital sodium. Its use should remain within the applicable professional veterinary and regulatory framework.
How should Dolethal be stored?
Storage should follow the current product label and national product information. Professional users should also comply with any applicable controlled-drug storage requirements.
Can Dolethal be shipped internationally?
International shipment depends on the laws of both the sending and receiving jurisdictions. Prescription, controlled-drug, importation, and veterinary pharmaceutical requirements may apply.
What should I check when receiving Dolethal 100ml?
Check the product name, concentration, vial size, manufacturer, batch number, expiry date, packaging integrity, and regulatory labeling before accepting the product.
Final Summary
Dolethal 100ml is a veterinary injectable solution containing pentobarbital sodium at 200 mg/ml in the formulation documented by current official product information. A 100 ml vial is an authorized presentation in certain markets, including the UK and Ireland.
The product is intended for veterinary euthanasia and is subject to prescription and regulatory controls. Its authorized target species and available package sizes can vary by jurisdiction, so international buyers should verify the applicable national authorization before purchasing or importing it.
For World Equine Vet, Dolethal 100ml should be positioned as a professional veterinary pharmaceutical product, with emphasis on verified product specifications, legitimate veterinary supply, regulatory compliance, and responsible professional use rather than unrestricted consumer purchasing.
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