Details for New Drug Application (NDA): 077267
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The generic ingredient in ZIDOVUDINE is zidovudine. There is one drug master file entry for this compound. Four suppliers are listed for this compound. Additional details are available on the zidovudine profile page.
Summary for 077267
| Tradename: | ZIDOVUDINE |
| Applicant: | Aurobindo |
| Ingredient: | zidovudine |
| Patents: | 0 |
Pharmacology for NDA: 077267
| Mechanism of Action | Nucleoside Reverse Transcriptase Inhibitors |
Medical Subject Heading (MeSH) Categories for 077267
Suppliers and Packaging for NDA: 077267
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ZIDOVUDINE | zidovudine | TABLET;ORAL | 077267 | ANDA | Aurobindo Pharma Limited | 65862-024 | 65862-024-10 | 6 BLISTER PACK in 1 CARTON (65862-024-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
| ZIDOVUDINE | zidovudine | TABLET;ORAL | 077267 | ANDA | Aurobindo Pharma Limited | 65862-024 | 65862-024-60 | 60 TABLET, FILM COATED in 1 BOTTLE (65862-024-60) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 300MG | ||||
| Approval Date: | Sep 19, 2005 | TE: | AB | RLD: | No | ||||
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