Meprobamate (Watson Laboratories, Inc.)


Welcome to the PulseAid listing for the Meprobamate drug offered from Watson Laboratories, Inc.. This 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: Meprobamate
SUBSTANCE NAME: MEPROBAMATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 1973-05-03
END MARKETING DATE: 0000-00-00


Meprobamate HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMeprobamate from Watson Laboratories, Inc.
LABELER NAME: Watson Laboratories, Inc.
DEA SCHEDULE: CIV
ACTIVE STRENGTH: 400(mg/1)
START MARKETING DATE: 1973-05-03
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0591-5238_102552df-6770-42a0-b488-87e57abb12c0
PRODUCT NDC: 0591-5238
APPLICATION NUMBER: ANDA083308

Other MEPROBAMATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Alembic Pharmaceuticals Inc.Meprobamate
Alembic Pharmaceuticals LimitedMEPROBAMATE
Avera McKennan HospitalMeprobamate
Dr.Reddy’s Laboratories LimitedMeprobamate
Heritage Pharmaceuticals Inc.Meprobamate
Taro Pharmaceutical Industries Ltd.Meprobamate
Taro Pharmaceuticals U.S.A., Inc.Meprobamate
Watson Laboratories, Inc.Meprobamate