Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 070476
Company: MCNEIL
Company: MCNEIL
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
IBUPROFEN | IBUPROFEN | 600MG | TABLET;ORAL | Discontinued | None | No | No |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
12/30/1988 | SUPPL-1 | Labeling |
Label is not available on this site. |