Details for New Drug Application (NDA): 212579
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The generic ingredient in ATAZANAVIR SULFATE is atazanavir sulfate. There are twenty-five drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the atazanavir sulfate profile page.
Summary for 212579
| Tradename: | ATAZANAVIR SULFATE |
| Applicant: | Laurus |
| Ingredient: | atazanavir sulfate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 212579
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ATAZANAVIR SULFATE | atazanavir sulfate | CAPSULE;ORAL | 212579 | ANDA | Laurus Labs Limited | 42385-920 | 42385-920-48 | 10 BLISTER PACK in 1 CARTON (42385-920-48) / 6 CAPSULE in 1 BLISTER PACK (42385-920-06) |
| ATAZANAVIR SULFATE | atazanavir sulfate | CAPSULE;ORAL | 212579 | ANDA | Laurus Labs Limited | 42385-920 | 42385-920-60 | 60 CAPSULE in 1 BOTTLE (42385-920-60) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 150MG BASE | ||||
| Approval Date: | Apr 30, 2021 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 200MG BASE | ||||
| Approval Date: | Apr 30, 2021 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 300MG BASE | ||||
| Approval Date: | Apr 30, 2021 | TE: | AB | RLD: | No | ||||
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