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Nitrofurantoin (monohydrate/macrocrystals)

NDC 70518-1087 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA077066
Dosage form / routeCAPSULE · ORAL
Active ingredientsNITROFURANTOIN (25 mg/1)
NITROFURANTOIN MONOHYDRATE (75 mg/1)
Marketing started20180329
Package count1

External sources

Source: openFDA. Public-domain (CC0).