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Nitrofurantoin (monohydrate/macrocrystals)

NDC 68071-4367 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077066
Dosage form / routeCAPSULE · ORAL
Active ingredientsNITROFURANTOIN (25 mg/1)
NITROFURANTOIN MONOHYDRATE (75 mg/1)
Marketing started20050406
Package count3

External sources

Source: openFDA. Public-domain (CC0).