FDA NDC Directory · JSON-LD · Markdown

Sildenafil

NDC 72865-105 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerXLCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203623
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (20 mg/1)
Marketing started20190710
Package count1

External sources

Source: openFDA. Public-domain (CC0).