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Betamethasone Dipropionate

NDC 0168-0268 · HUMAN PRESCRIPTION DRUG · OINTMENT, AUGMENTED

Generic namebetamethasone dipropionate
Labeler / ManufacturerE. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075373
Dosage form / routeOINTMENT, AUGMENTED · TOPICAL
Active ingredientsBETAMETHASONE DIPROPIONATE (.5 mg/g)
Marketing started19990622
Package count2

External sources

Source: openFDA. Public-domain (CC0).