Ombitasvir/Paritaprevir/Ritonavir + Dasabuvir Suppliers & Bulk Manufacturers
Available Forms: Tablet
Available Strengths: Ombitasvir 12.5 mg / Paritaprevir 75 mg / Ritonavir 50 mg (tablet)+ Dasabuvir 250 mg (tablet)
Reference Brands: Viekira Pak® (US); Viekirax® + Exviera® (EU)
Category: Hepatitis
Ombitasvir/Paritaprevir/Ritonavir + Dasabuvir, marketed as Viekira Pak® (US) and Viekirax® + Exviera® (EU), is a fixed-dose oral combination for Hepatitis C genotype 1. Approved by FDA and EMA, it offers an effective interferon-free treatment option, often used with ribavirin in B2B supply for global pharmaceutical markets.
Product Description:
Ombitasvir/Paritaprevir/Ritonavir + Dasabuvir is a fixed-dose combination therapy used in the treatment of chronic Hepatitis C genotype 1. Marketed as Viekira Pak® in the US and Viekirax® + Exviera® in the EU, this regimen includes four direct-acting antivirals that target multiple stages of the HCV replication cycle. It offers a non-interferon-based treatment, often in combination with ribavirin. EMA and FDA approved, it’s a key option for B2B pharmaceutical partners sourcing branded and generic HCV therapies. Suitable for hospital, retail, and tender supply in regulated and semi-regulated markets. Available in tablet form with clearly defined daily dosing.
Ombitasvir/Paritaprevir/Ritonavir + Dasabuvir — third party manufacturing & bulk supply
Ombitasvir/Paritaprevir/Ritonavir + Dasabuvir is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:
What to include when you enquire
- Destination market — determines which manufacturers hold the right site-level approvals
- First order quantity and estimated annual volume
- Whether you need a registration dossier or the product is already registered
- Packaging, labelling and language requirements
- Incoterms and required shelf life
Manufacturers of Ombitasvir/Paritaprevir/Ritonavir + Dasabuvir listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding. Narcotic drugs and controlled substances are supplied strictly against valid import and export permits issued by the competent authorities.
Request a quote for Ombitasvir/Paritaprevir/Ritonavir + Dasa... →The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
Frequently Asked Questions
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