Active Ingredient: NITROFURANTOIN, MACROCRYSTALLINE
Proprietary Name: NITROFURANTOIN MACROCRYSTALLINE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070248
Product Number: 001
Approval Date: Jun 24, 1988
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information