NDC 71335-2320 – Nitrofurantoin

Nitrofurantoin 25 mg/1; Nitrofurantoin Monohydrate 75 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2320

Product details

Brand name
Nitrofurantoin
Generic name
Nitrofurantoin
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA208516
Marketed since
January 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
Nitrofuran Antibacterial; Nitrofuran Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Nitrofurantoin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2320-06 CAPSULE in 1 BOTTLE (71335-2320-0)Jan 4, 2024
71335-2320-120 CAPSULE in 1 BOTTLE (71335-2320-1)Jan 4, 2024
71335-2320-214 CAPSULE in 1 BOTTLE (71335-2320-2)Jan 4, 2024
71335-2320-330 CAPSULE in 1 BOTTLE (71335-2320-3)Jan 4, 2024
71335-2320-428 CAPSULE in 1 BOTTLE (71335-2320-4)Jan 4, 2024
71335-2320-560 CAPSULE in 1 BOTTLE (71335-2320-5)Jan 4, 2024
71335-2320-610 CAPSULE in 1 BOTTLE (71335-2320-6)Jan 4, 2024
71335-2320-790 CAPSULE in 1 BOTTLE (71335-2320-7)Jan 4, 2024
71335-2320-821 CAPSULE in 1 BOTTLE (71335-2320-8)Jan 4, 2024
71335-2320-98 CAPSULE in 1 BOTTLE (71335-2320-9)Jan 4, 2024

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