Naloxone Hydrochloride (McKesson Packaging Services Business Unit of McKesson Corporation)
Welcome to the PulseAid listing for the Naloxone Hydrochloride drug offered from McKesson Packaging Services Business Unit of McKesson Corporation. 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: | McKesson Packaging Services Business Unit of McKesson Corporation |
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: | 2010-05-03 |
END MARKETING DATE: | 0000-00-00 |
Naloxone Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Naloxone Hydrochloride from McKesson Packaging Services Business Unit of McKesson Corporation |
LABELER NAME: | McKesson Packaging Services Business Unit of McKesson Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.4(mg/mL) |
START MARKETING DATE: | 2010-05-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63739-463_1a757301-419a-457e-9989-cdf57c902988 |
PRODUCT NDC: | 63739-463 |
APPLICATION NUMBER: | ANDA070254 |
Other NALOXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: