DrugPatentWatch Database Preview
Atazanavir - Generic Drug Details
» See Plans and Pricing
Generic filers with tentative approvals for ATAZANAVIR
Applicant | Application No. | Strength | Dosage Form |
Start Trial | Start Trial | 300MG/100MG | TABLET; ORAL |
Start Trial | Start Trial | 200MG | CAPSULE; ORAL |
Start Trial | Start Trial | 150MG | CAPSULE; ORAL |
The 'tentative' approval signifies that the product meets all FDA standards for marketing, and, but for the patents / regulatory protections, it would approved.
US Patents and Regulatory Information for atazanavir
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Teva Pharms Usa | ATAZANAVIR SULFATE | atazanavir sulfate | CAPSULE;ORAL | 091673-004 | Apr 22, 2014 | AB | RX | No | No | Start Trial | Start Trial | Start Trial | |||
Mylan | ATAZANAVIR SULFATE | atazanavir sulfate | CAPSULE;ORAL | 208177-001 | Sep 24, 2018 | DISCN | No | No | Start Trial | Start Trial | Start Trial | ||||
Bristol Myers Squibb | REYATAZ | atazanavir sulfate | CAPSULE;ORAL | 021567-004 | Oct 16, 2006 | AB | RX | Yes | Yes | Start Trial | Start Trial | Start Trial | |||
Bristol-myers Squibb | EVOTAZ | atazanavir sulfate; cobicistat | TABLET;ORAL | 206353-001 | Jan 29, 2015 | RX | Yes | Yes | Start Trial | Start Trial | Y | Y | Start Trial | ||
Bristol Myers Squibb | REYATAZ | atazanavir sulfate | CAPSULE;ORAL | 021567-003 | Jun 20, 2003 | AB | RX | Yes | No | Start Trial | Start Trial | Start Trial | |||
Amneal | ATAZANAVIR SULFATE | atazanavir sulfate | CAPSULE;ORAL | 209717-002 | Jun 1, 2020 | AB | RX | No | No | Start Trial | Start Trial | Start Trial | |||
Amneal | ATAZANAVIR SULFATE | atazanavir sulfate | CAPSULE;ORAL | 209717-004 | Jun 1, 2020 | AB | RX | No | No | Start Trial | Start Trial | Start Trial | |||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |