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 Description | Meprobamate 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: