NDC 0185-0122 – Nitrofurantoin (monohydrate/macrocrystals)

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

Human Prescription Drug 1 recall

Product NDC0185-0122

Product details

Brand name
Nitrofurantoin (monohydrate/macrocrystals)
Generic name
Nitrofurantoin (monohydrate/macrocrystals)
Labeler
Sandoz Inc
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077066
Marketed since
April 6, 2005
Listing expires
December 31, 2026
Pharmacologic class
Nitrofuran Antibacterial; Nitrofuran Antibacterial

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0185-0122-01100 CAPSULE in 1 BOTTLE (0185-0122-01)Apr 6, 2005
0185-0122-101000 CAPSULE in 1 BOTTLE (0185-0122-10)Apr 6, 2005

Recalls mentioning this NDC

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