Generics 13

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Atazanavir manufacturers

13 products found

Filters

13 products found

atazanavir

Capsules 100 mg, 150 mg, 200 mg, 300 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP
Unavailable markets
Vietnam
Manufacturer #519

Manufacturer usually replies in 6 days

atazanavir

Capsules 200 mg, 300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP, WHO
Manufacturer #2303

Manufacturer usually replies in 7 days

atazanavir + ritonavir

Tablets 300 mg + 100 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
GMP, WHO
Manufacturer #24869

Manufacturer usually replies in 3 days

atazanavir

Capsules 300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
GMP, WHO
Manufacturer #24869

Manufacturer usually replies in 3 days

atazanavir

Tablets 100 mg, 150 mg, 200 mg, 300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20401

Manufacturer usually replies in 5 days

atazanavir

Capsules 100 mg, 150 mg, 200 mg, 300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20401

Manufacturer usually replies in 5 days

atazanavir

Tablets for oral solution 150 mg, 200 mg, 300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #19844

Manufacturer usually replies in 9 days

atazanavir + ritonavir

Tablets 300 mg+100 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #19725

Manufacturer usually replies in 6 days

atazanavir + ritonavir

Tablets 300 mg+100 mg

Dossier type
CTD
Dossier status
Under development
Country of origin
India
GMP approvals
WHO
Manufacturer #19670

Manufacturer usually replies in 8 days

atazanavir

Capsules 150 mg, 200 mg, 300 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Unavailable markets
Chile , Turkey , Vietnam , Panama
Available for
Licensing with supply
Manufacturer #261
A pharmaceutical manufacturer based in the EU that has been selling its products in Europe for 20+ years. Main therapeutic areas include diabetes, CNL, dermatology, and oncology. Main dosage forms include solid and liquid oral, sterile dosage forms, and ointments. The company possesses 10+ manufacturing facilities that are cGMP-compliant.

Manufacturer usually replies in 6 days

atazanavir

Capsules 300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #19828

Manufacturer usually replies in 14 days

atazanavir

Tablets 150 mg+300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #19820

Manufacturer usually replies in 11 days

atazanavir

Capsules 100 mg, 150 mg, 200 mg, 300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #21324

Manufacturer usually replies in nan days

ATAZANAVIR Manufacturers and Suppliers

We have found 5 verified atazanavir manufacturers and atazanavir suppliers from our global list of sellers. The pharmaceutical drug is available for sale in different forms such as capsules, tablets from manufacturers in various countries including European Union, India, Russia.

Navigating our pharmaceutical marketplace

Being a global B2B pharmaceutical online marketplace, Pipelinepharma is structured to simplify pharmaceutical deals by providing you with an intuitive interface that is easy to engage with. The selection of atazanavir offerings can be narrowed down with the use of filters and easily weighed against one another according to medication prices and commercial terms. The advanced filters help you filter out the countries for atazanavir manufacturers and atazanavir suppliers that you are looking for. These also enable you to check the dossier status of atazanavir, and the GMP approvals of the different variants of atazanavir. Also, each manufacturer or supplier product description contains essential information about atazanavir including clinical data, stability zones, countries where atazanavir is already registered in. Manufacturers also specify the commercial terms of their offers, such as the market for which the offer is intended, deal type, dossier licensing fee, supply price, payment terms, and delivery terms.

Establishing commercial ties

If you are a pharmaceutical licensing company or a distributor you can enter into deals or negotiations over atazanavir offers with manufacturing companies after completing the free registration process and joining our online marketplace. This helps to ensure that you conclude the pharmaceutical deal at a reasonable cost and achieve the best cost/benefit ratio for your company while bypassing lengthy sourcing, negotiation, and ordering process. Once you have finalized a deal, you can look forward to a long-lasting business relationship with the manufacturers or suppliers. This way, the marketplace allows you as a distributor to skip the process of shortlisting product manufacturers every time you are looking for in-licensing or distribution deals.

Quality Assurance

To keep up to the quality standards other than Good Manufacturing Practice approvals that atazanavir manufacturers have, we qualify their companies before they are on-boarded on the platform. This allows us to screen atazanavir manufacturers for the quality of the pharmaceutical products’ dossiers and protect against the risk of possible malpractices.