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Betamethasone Dipropionate

NDC 0168-0267 · HUMAN PRESCRIPTION DRUG · LOTION, AUGMENTED

Labeler / ManufacturerE. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077111
Dosage form / routeLOTION, AUGMENTED · TOPICAL
Active ingredientsBETAMETHASONE DIPROPIONATE (.5 mg/mL)
Marketing started20070521
Package count2

External sources

Source: openFDA. Public-domain (CC0).