Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 007392
Company: LILLY
Company: LILLY
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| SECONAL SODIUM | SECOBARBITAL SODIUM | 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION | Discontinued | None | No | No |
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
|---|---|---|---|---|---|---|---|
| 07/19/1950 | ORIG-1 | Approval | Type 2 - New Active Ingredient | STANDARD |
Label is not available on this site. |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 04/05/1982 | SUPPL-6 | Labeling |
Label is not available on this site. |
||
| 06/24/1981 | SUPPL-5 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 07/23/1974 | SUPPL-3 | Unspecified |
Label is not available on this site. |