Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 009436
Company: NOVARTIS
Company: NOVARTIS
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| ACYLANID | ACETYLDIGITOXIN | 0.1MG | TABLET;ORAL | Discontinued | None | No | No |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 01/06/1981 | SUPPL-9 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
||
| 08/02/1977 | SUPPL-7 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
| 04/27/1978 | SUPPL-6 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
||
| 04/16/1976 | SUPPL-5 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
| 04/24/1975 | SUPPL-4 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |