FDA NDC Directory · JSON-LD · Markdown

Nitrofurantoin

NDC 70069-829 · HUMAN PRESCRIPTION DRUG · FOR SUSPENSION

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208909
Dosage form / routeFOR SUSPENSION · ORAL
Active ingredientsNITROFURANTOIN (25 mg/5mL)
Marketing started20250226
Package count1

External sources

Source: openFDA. Public-domain (CC0).