Chlorpromazine Hydrochloride (Sandoz Inc)
Welcome to the PulseAid listing for the Chlorpromazine Hydrochloride drug offered from Sandoz 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: | Sandoz Inc |
NON-PROPRIETARY NAME: | Chlorpromazine Hydrochloride |
SUBSTANCE NAME: | CHLORPROMAZINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, SUGAR COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1974-07-09 |
END MARKETING DATE: | 0000-00-00 |
Chlorpromazine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Chlorpromazine Hydrochloride from Sandoz Inc |
LABELER NAME: | Sandoz Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/1) |
START MARKETING DATE: | 1974-07-09 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0781-5913_9d59dceb-83c5-4043-a2b7-96fe6511ecfe |
PRODUCT NDC: | 0781-5913 |
APPLICATION NUMBER: | ANDA083386 |
Other CHLORPROMAZINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: