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betamethasone dipropionate

NDC 70771-1550 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214048
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsBETAMETHASONE DIPROPIONATE (.5 mg/g)
Marketing started20200720
Package count2

External sources

Source: openFDA. Public-domain (CC0).