FDA NDC Directory · JSON-LD · Markdown

Nitrofurantion

NDC 57664-232 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201722
Dosage form / routeCAPSULE · ORAL
Active ingredientsNITROFURANTOIN (50 mg/1)
Marketing started20160415
Package count2

External sources

Source: openFDA. Public-domain (CC0).