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Metronidazole

NDC 71335-1922 · Bryant Ranch Prepack

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

Packages

71335-1922-0 40 TABLET in 1 BOTTLE (71335-1922-0)

71335-1922-1 20 TABLET in 1 BOTTLE (71335-1922-1)

71335-1922-2 30 TABLET in 1 BOTTLE (71335-1922-2)

71335-1922-3 14 TABLET in 1 BOTTLE (71335-1922-3)

71335-1922-4 56 TABLET in 1 BOTTLE (71335-1922-4)

71335-1922-5 21 TABLET in 1 BOTTLE (71335-1922-5)

71335-1922-6 4 TABLET in 1 BOTTLE (71335-1922-6)

71335-1922-7 28 TABLET in 1 BOTTLE (71335-1922-7)

71335-1922-8 100 TABLET in 1 BOTTLE (71335-1922-8)

71335-1922-9 60 TABLET in 1 BOTTLE (71335-1922-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70771-1834 — Metronidazole, 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, 71335-2640 — 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, 72162-2678 — 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.