Naloxone Hydrochloride (Somerset Therapeutics, LLC)
Welcome to the PulseAid listing for the Naloxone Hydrochloride drug offered from Somerset Therapeutics, LLC. 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: | Somerset Therapeutics, LLC |
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: | 2017-08-10 |
END MARKETING DATE: | 0000-00-00 |
Naloxone Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Naloxone Hydrochloride from Somerset Therapeutics, LLC |
LABELER NAME: | Somerset Therapeutics, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.4(mg/mL) |
START MARKETING DATE: | 2017-08-10 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 70069-071_d8b851af-3f2a-495e-85d6-61167e3b288b |
PRODUCT NDC: | 70069-071 |
APPLICATION NUMBER: | ANDA207633 |
Other NALOXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: