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Butenafine Hydrochloride

NDC 73581-210 · HUMAN OTC DRUG · CREAM

Labeler / ManufacturerYYBA CORP
Marketing categoryAbbreviated NDA (generic) · App ANDA205181
Dosage form / routeCREAM · TOPICAL
Active ingredientsBUTENAFINE HYDROCHLORIDE (10 mg/g)
Marketing started20231012
Package count1

External sources

Source: openFDA. Public-domain (CC0).