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 DescriptionAMMONIUM LACTATE from Watson Laboratories, Inc.
LABELER NAME: Watson Laboratories, Inc.
DEA SCHEDULE:
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:

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