IBUPROFEN (IBUPROFEN) — FDA Approval ANDA071905 (WATSON LABS)
IBUPROFEN (IBUPROFEN) — FDA Approval ANDA071905 (WATSON LABS) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: IBUPROFEN; Active ingredients: IBUPROFEN; Application number: ANDA071905.
| Brand name | IBUPROFEN |
|---|---|
| Active ingredients | IBUPROFEN |
| Application number | ANDA071905 |
| Sponsor | WATSON LABS |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19980721 |
| Source | openFDA Drugs@FDA |
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