Ketamine Hydrochloride (Hospira, Inc.)
Welcome to the PulseAid listing for the Ketamine Hydrochloride drug offered from Hospira, Inc.. This General Anesthesia [PE],General Anesthetic [EPC] 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: | Hospira, Inc. |
| NON-PROPRIETARY NAME: | KETAMINE HYDROCHLORIDE |
| SUBSTANCE NAME: | KETAMINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | General Anesthesia [PE],General Anesthetic [EPC] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2004-11-30 |
| END MARKETING DATE: | 0000-00-00 |
Ketamine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Ketamine Hydrochloride from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 100(mg/mL) |
| START MARKETING DATE: | 2004-11-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-2051_80dbd0eb-8c4d-4b1b-8722-497177d58ec7 |
| PRODUCT NDC: | 0409-2051 |
| APPLICATION NUMBER: | ANDA074549 |
Other KETAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
