NDC 16571-888 – Nitrofurantoin

Nitrofurantoin 50 mg/5mL · Suspension · Oral

Human Prescription Drug

Product NDC16571-888

Product details

Brand name
Nitrofurantoin
Generic name
Nitrofurantoin
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Suspension
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA009175
Marketed since
February 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Nitrofuran Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Nitrofurantoin →

Package NDC codes (1)

Package NDCDescriptionSince
16571-888-061 BOTTLE in 1 CARTON (16571-888-06) / 60 mL in 1 BOTTLEFeb 1, 2024

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