NEOSTIGMINE METHYLSULFATE (Amphastar Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the NEOSTIGMINE METHYLSULFATE drug offered from Amphastar Pharmaceuticals, Inc.. This Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [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: | Amphastar Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | neostigmine methylsulfate |
SUBSTANCE NAME: | NEOSTIGMINE METHYLSULFATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2017-09-25 |
END MARKETING DATE: | 0000-00-00 |
NEOSTIGMINE METHYLSULFATE HUMAN PRESCRIPTION DRUG Details:
Item Description | NEOSTIGMINE METHYLSULFATE from Amphastar Pharmaceuticals, Inc. |
LABELER NAME: | Amphastar Pharmaceuticals, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.5(mg/mL) |
START MARKETING DATE: | 2017-09-25 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0548-9601_e4f0003a-c0f1-4784-8dfd-2d9a849ade9f |
PRODUCT NDC: | 0548-9601 |
APPLICATION NUMBER: | ANDA209933 |
Other NEOSTIGMINE METHYLSULFATE Pharmaceutical Manufacturers / Labelers: