FDA NDC Directory · JSON-LD · Markdown

Betamethasone dipropionate

NDC 51672-1390 · HUMAN PRESCRIPTION DRUG · SPRAY

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211722
Dosage form / routeSPRAY · TOPICAL
Active ingredientsBETAMETHASONE DIPROPIONATE (.5 mg/g)
Marketing started20200617
Package count2

External sources

Source: openFDA. Public-domain (CC0).