Nembutal Sodium (Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.))
Welcome to the PulseAid listing for the Nembutal Sodium drug offered from Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.). This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| NON-PROPRIETARY NAME: | pentobarbital sodium |
| SUBSTANCE NAME: | PENTOBARBITAL SODIUM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1973-09-19 |
| END MARKETING DATE: | 0000-00-00 |
Nembutal Sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Nembutal Sodium from Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| LABELER NAME: | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 50(mg/mL) |
| START MARKETING DATE: | 1973-09-19 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 76478-501_d2e78e41-8a39-42ca-a6a4-375b5db85635 |
| PRODUCT NDC: | 76478-501 |
| APPLICATION NUMBER: | ANDA083246 |
Other PENTOBARBITAL SODIUM Pharmaceutical Manufacturers / Labelers:
