Naloxone Hydrochloride (Hospira, Inc.)
Welcome to the PulseAid listing for the Naloxone Hydrochloride drug offered from Hospira, Inc.. This Opioid Antagonist [EPC],Opioid Antagonists [MoA] 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: | NALOXONE HYDROCHLORIDE |
| SUBSTANCE NAME: | NALOXONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2005-07-12 |
| END MARKETING DATE: | 0000-00-00 |
Naloxone Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Naloxone Hydrochloride from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.4(mg/mL) |
| START MARKETING DATE: | 2005-07-12 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-1215_69f4369e-9438-4faf-afcd-d4a417acae9d |
| PRODUCT NDC: | 0409-1215 |
| APPLICATION NUMBER: | ANDA070256 |
Other NALOXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
