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Metronidazole

NDC 72162-2678 · Bryant Ranch Prepack

Generic nameMetronidazole
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)METRONIDAZOLE
Strength500 mg/1
Pharmacologic classNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
Marketing categoryANDA

Packages

72162-2678-1 — 100 TABLET, FILM COATED in 1 BOTTLE (72162-2678-1)

72162-2678-2 — 50 TABLET, FILM COATED in 1 BOTTLE (72162-2678-2)

72162-2678-5 — 500 TABLET, FILM COATED in 1 BOTTLE (72162-2678-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-1922 — Metronidazole, 71335-2640 — Metronidazole, 71335-2681 — metronidazole, 71335-2949 — metronidazole, 71656-066 — Metronidazole Oral, 71656-067 — metronidazole, 72162-2259 — Metronidazole, 72162-2403 — Metronidazole, 72162-2468 — metronidazole, 72162-2677 — Metronidazole, 72572-540 — Metronidazole, 72578-007 — metronidazole, 72578-008 — metronidazole, 72578-129 — Metronidazole, 72578-209 — Metronidazole, 72789-005 — Metronidazole, 72789-007 — Metronidazole, 72789-011 — Metronidazole, 72789-195 — metronidazole, 73473-303 — Metronidazole, +161 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.