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BETAMETHASONE DIPROPIONATE

NDC 59651-699 · HUMAN PRESCRIPTION DRUG · OINTMENT, AUGMENTED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218289
Dosage form / routeOINTMENT, AUGMENTED · TOPICAL
Active ingredientsBETAMETHASONE DIPROPIONATE (.5 mg/g)
Marketing started20240410
Package count3

External sources

Source: openFDA. Public-domain (CC0).