Prochlorperazine (G&W Laboratories, Inc.)
Welcome to the PulseAid listing for the Prochlorperazine drug offered from G&W Laboratories, Inc.. This Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] 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: | G&W Laboratories, Inc. |
NON-PROPRIETARY NAME: | Prochlorperazine |
SUBSTANCE NAME: | PROCHLORPERAZINE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
ROUTE: | RECTAL |
DOSAGE FORM: | SUPPOSITORY |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1993-11-30 |
END MARKETING DATE: | 0000-00-00 |
Prochlorperazine HUMAN PRESCRIPTION DRUG Details:
Item Description | Prochlorperazine from G&W Laboratories, Inc. |
LABELER NAME: | G&W Laboratories, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 25(mg/1) |
START MARKETING DATE: | 1993-11-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0713-0135_9b40b2be-7999-65e4-7923-4fd9afe64284 |
PRODUCT NDC: | 0713-0135 |
APPLICATION NUMBER: | ANDA040058 |
Other PROCHLORPERAZINE Pharmaceutical Manufacturers / Labelers: