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Metronidazole

NDC 70518-3265 · REMEDYREPACK INC.

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

Packages

70518-3265-1 — 4 TABLET in 1 BOTTLE, PLASTIC (70518-3265-1)

70518-3265-2 — 14 TABLET in 1 BOTTLE, PLASTIC (70518-3265-2)

70518-3265-4 — 20 TABLET in 1 BOTTLE, PLASTIC (70518-3265-4)

70518-3265-5 — 30 TABLET in 1 BLISTER PACK (70518-3265-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-0058 — Metronidazole, 70518-0088 — Metronidazole, 70518-1240 — Metronidazole, 70518-1241 — Metronidazole, 70518-1536 — Metronidazole, 70518-2305 — Metronidazole, 70518-2663 — metronidazole, 70518-2814 — metronidazole, 70518-3042 — metronidazole, 70518-3110 — Metronidazole, 70518-4495 — Metronidazole, 70518-4572 — metronidazole, 70771-1045 — METRONIDAZOLE, 70771-1046 — METRONIDAZOLE, 70771-1834 — Metronidazole, 70771-1978 — Metronidazole, 71209-062 — Metronidazole, 71209-063 — Metronidazole, 71335-0358 — Metronidazole, 71335-0858 — 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.