Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 010441
Company: EVERYLIFE
Company: EVERYLIFE
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
RESERPINE | RESERPINE | 0.1MG | TABLET;ORAL | Discontinued | None | No | No |
RESERPINE | RESERPINE | 0.25MG | TABLET;ORAL | Discontinued | None | No | No |
RESERPINE | RESERPINE | 0.5MG | TABLET;ORAL | Discontinued | None | No | No |
RESERPINE | RESERPINE | 1MG | TABLET;ORAL | Discontinued | None | No | No |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
01/03/1980 | SUPPL-7 | Labeling |
Label is not available on this site. |
||
02/21/1978 | SUPPL-6 | Manufacturing (CMC)-Control |
Label is not available on this site. |