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Metronidazole

NDC 71335-2640 · 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

71335-2640-1 — 14 TABLET, FILM COATED in 1 BOTTLE (71335-2640-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70771-1978 — Metronidazole, 71209-062 — Metronidazole, 71209-063 — Metronidazole, 71335-0358 — Metronidazole, 71335-0858 — Metronidazole, 71335-1681 — Metronidazole, 71335-1703 — metronidazole, 71335-1775 — metronidazole, 71335-1838 — Metronidazole, 71335-1922 — 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, 72162-2678 — Metronidazole, 72572-540 — 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.