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BETAMETHASONE DIPROPIONATE

NDC 35573-107 · HUMAN PRESCRIPTION DRUG · OINTMENT, AUGMENTED

Labeler / ManufacturerBurel Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218289
Dosage form / routeOINTMENT, AUGMENTED · TOPICAL
Active ingredientsBETAMETHASONE DIPROPIONATE (.5 mg/g)
Marketing started20250115
Package count2

External sources

Source: openFDA. Public-domain (CC0).