NDC 70518-1087 – Nitrofurantoin (monohydrate/macrocrystals)

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

Human Prescription Drug 1 recall

Product NDC70518-1087

Product details

Brand name
Nitrofurantoin (monohydrate/macrocrystals)
Generic name
Nitrofurantoin (monohydrate/macrocrystals)
Labeler
REMEDYREPACK INC.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077066
Marketed since
March 29, 2018
Listing expires
December 31, 2027
Pharmacologic class
Nitrofuran Antibacterial; Nitrofuran Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Nitrofurantoin (monohydrate/macrocrystals) →

Package NDC codes (1)

Package NDCDescriptionSince
70518-1087-110 CAPSULE in 1 BOTTLE, PLASTIC (70518-1087-1)Aug 16, 2018

Recalls mentioning this NDC

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