FDA NDC Directory · JSON-LD · Markdown

Sildenafil

NDC 31722-710 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202659
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSILDENAFIL CITRATE (50 mg/1)
Marketing started20180611
Package count3

External sources

Source: openFDA. Public-domain (CC0).