NDC 57664-231 – Nitrofurantion

Nitrofurantoin 25 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC57664-231

Product details

Brand name
Nitrofurantion
Generic name
Nitrofurantion
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA201722
Marketed since
April 15, 2016
Listing expires
December 31, 2027
Pharmacologic class
Nitrofuran Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Nitrofurantion →

Package NDC codes (2)

Package NDCDescriptionSince
57664-231-181000 CAPSULE in 1 BOTTLE (57664-231-18)Apr 15, 2016
57664-231-88100 CAPSULE in 1 BOTTLE (57664-231-88)Apr 15, 2016

Recalls mentioning this NDC

Other Nitrofurantion products