FDA NDC Directory · JSON-LD · Markdown

NITROFURANTOIN

NDC 72189-179 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerDirectrx
Marketing categoryAbbreviated NDA (generic) · App ANDA077066
Dosage form / routeCAPSULE · ORAL
Active ingredientsNITROFURANTOIN (25 mg/1)
NITROFURANTOIN MONOHYDRATE (75 mg/1)
Marketing started20220118
Package count3

External sources

Source: openFDA. Public-domain (CC0).