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Ammonium Lactate

NDC 45802-419 · HUMAN PRESCRIPTION DRUG · LOTION

Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA075570
Dosage form / routeLOTION · TOPICAL
Active ingredientsAMMONIUM LACTATE (12 g/100g)
Marketing started20060620
Package count2

External sources

Source: openFDA. Public-domain (CC0).