NDC 70069-829 – Nitrofurantoin

Nitrofurantoin 25 mg/5mL · For Suspension · Oral

Human Prescription Drug

Product NDC70069-829

Product details

Brand name
Nitrofurantoin
Generic name
Nitrofurantoin
Labeler
Somerset Therapeutics, LLC
Dosage form
For Suspension
Route
Oral
Marketing category
ANDA · ANDA208909
Marketed since
February 26, 2025
Listing expires
December 31, 2027
Pharmacologic class
Nitrofuran Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Nitrofurantoin →

Package NDC codes (1)

Package NDCDescriptionSince
70069-829-011 BOTTLE, GLASS in 1 CARTON (70069-829-01) / 230 mL in 1 BOTTLE, GLASSFeb 26, 2025

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