NDC 70518-0088 – Metronidazole

Metronidazole 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-0088

Product details

Brand name
Metronidazole
Generic name
Metronidazole
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203458
Marketed since
December 28, 2016
Listing expires
December 31, 2027
Pharmacologic class
Nitroimidazole Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Metronidazole →

Package NDC codes (5)

Package NDCDescriptionSince
70518-0088-014 TABLET, FILM COATED in 1 BLISTER PACK (70518-0088-0)Dec 28, 2016
70518-0088-214 TABLET, FILM COATED in 1 BOTTLE (70518-0088-2)Dec 30, 2016
70518-0088-34 TABLET, FILM COATED in 1 BOTTLE (70518-0088-3)Dec 30, 2016
70518-0088-430 TABLET, FILM COATED in 1 BLISTER PACK (70518-0088-4)Jan 31, 2017
70518-0088-521 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0088-5)May 13, 2019

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