Hydroxocobalamin (Watson Laboratories, Inc.)


Welcome to the PulseAid listing for the Hydroxocobalamin drug offered from Watson Laboratories, Inc.. This Antidote [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: Watson Laboratories, Inc.
NON-PROPRIETARY NAME: Hydroxocobalamin
SUBSTANCE NAME: HYDROXOCOBALAMIN ACETATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Antidote [EPC]
ROUTE: INTRAMUSCULAR
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2010-11-12
END MARKETING DATE: 0000-00-00


Hydroxocobalamin HUMAN PRESCRIPTION DRUG Details:

Item DescriptionHydroxocobalamin from Watson Laboratories, Inc.
LABELER NAME: Watson Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1000(ug/mL)
START MARKETING DATE: 2010-11-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0591-2888_8a32969f-18b7-4a22-8566-928b31b366f1
PRODUCT NDC: 0591-2888
APPLICATION NUMBER: ANDA085998

Other HYDROXOCOBALAMIN ACETATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Watson Laboratories, Inc.Hydroxocobalamin