Ammonium Lactate (Taro Pharmaceuticals U.S.A., Inc.)
Welcome to the PulseAid listing for the Ammonium Lactate drug offered from Taro Pharmaceuticals U.S.A., 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: | Taro Pharmaceuticals U.S.A., Inc. |
| NON-PROPRIETARY NAME: | Ammonium Lactate |
| SUBSTANCE NAME: | AMMONIUM LACTATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LOTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2004-05-28 |
| END MARKETING DATE: | 0000-00-00 |
Ammonium Lactate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Ammonium Lactate from Taro Pharmaceuticals U.S.A., Inc. |
| LABELER NAME: | Taro Pharmaceuticals U.S.A., Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 120(mg/g) |
| START MARKETING DATE: | 2004-05-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51672-1300_b2dec930-0ae6-4f5d-b143-1b9a6f32cc35 |
| PRODUCT NDC: | 51672-1300 |
| APPLICATION NUMBER: | ANDA076216 |
Other AMMONIUM LACTATE Pharmaceutical Manufacturers / Labelers: