NDC 68788-8674 – Metronidazole

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

Human Prescription Drug

Product NDC68788-8674

Product details

Brand name
Metronidazole
Generic name
Metronidazole
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203458
Marketed since
May 23, 2024
Listing expires
December 31, 2027
Pharmacologic class
Nitroimidazole Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Metronidazole →

Package NDC codes (6)

Package NDCDescriptionSince
68788-8674-114 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-1)May 23, 2024
68788-8674-221 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-2)May 23, 2024
68788-8674-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-3)May 23, 2024
68788-8674-428 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-4)May 23, 2024
68788-8674-556 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-5)May 23, 2024
68788-8674-742 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-7)May 23, 2024

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