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 DescriptionAmmonium 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:

Manufacturer / LabelerProprietary Name
Nnodum PharmaceuticalsAmmonium Lactate
Perrigo New York IncAmmonium Lactate
Physicians Total Care, Inc.Ammonium Lactate
Ranbaxy Laboratories Inc.Lac-Hydrin
Taro Pharmaceuticals U.S.A., Inc.Ammonium Lactate
Watson Laboratories, Inc.AMMONIUM LACTATE