AMMONIUM LACTATE (Watson Laboratories, Inc.)
Welcome to the PulseAid listing for the AMMONIUM LACTATE 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: | AMMONIUM LACTATE |
SUBSTANCE NAME: | AMMONIUM LACTATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2012-06-05 |
END MARKETING DATE: | 0000-00-00 |
AMMONIUM LACTATE HUMAN PRESCRIPTION DRUG Details:
Item Description | AMMONIUM LACTATE from Watson Laboratories, Inc. |
LABELER NAME: | Watson Laboratories, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 12(g/100g) |
START MARKETING DATE: | 2012-06-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0591-2157_df534055-c02c-41e9-a81c-72ed70eff9e4 |
PRODUCT NDC: | 0591-2157 |
APPLICATION NUMBER: | ANDA075774 |
Other AMMONIUM LACTATE Pharmaceutical Manufacturers / Labelers: