FDA NDC Directory · JSON-LD · Markdown

Oxybutynin Chloride

NDC 51655-665 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209823
Dosage form / routeTABLET · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (5 mg/1)
Marketing started20220809
Package count2

External sources

Source: openFDA. Public-domain (CC0).