IBUPROFEN (IBUPROFEN) — FDA Approval ANDA077338 (P AND L DEV LLC)
IBUPROFEN (IBUPROFEN) — FDA Approval ANDA077338 (P AND L DEV LLC) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: IBUPROFEN; Active ingredients: IBUPROFEN; Application number: ANDA077338.
| Brand name | IBUPROFEN |
|---|---|
| Active ingredients | IBUPROFEN |
| Application number | ANDA077338 |
| Sponsor | P AND L DEV LLC |
| Dosage form | CAPSULE |
| Route | ORAL |
| Marketing status | Over-the-counter |
| Products in application | 1 |
| First approval date | 20090710 |
| Source | openFDA Drugs@FDA |
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