Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 011679
Company: ABBOTT
Company: ABBOTT
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| PENTOTHAL | THIOPENTAL SODIUM | 400MG/GM | SUSPENSION;RECTAL | 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 |
|---|---|---|---|---|---|---|---|
| 09/23/1959 | ORIG-1 | Approval | Type 1 - New Molecular Entity | PRIORITY |
Label is not available on this site. |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 03/30/1995 | SUPPL-18 | Labeling |
Label is not available on this site. |
||
| 09/17/2001 | SUPPL-17 | Labeling |
Label is not available on this site. |
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| 02/15/1984 | SUPPL-13 | Labeling |
Label is not available on this site. |
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| 01/24/1977 | SUPPL-10 | Labeling |
Label is not available on this site. |
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| 09/10/1976 | SUPPL-9 | Labeling |
Label is not available on this site. |
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| 10/20/1975 | SUPPL-7 | Labeling |
Label is not available on this site. |
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| 08/30/1971 | SUPPL-6 | Labeling |
Label is not available on this site. |