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metronidazole

NDC 70518-3042 · REMEDYREPACK INC.

Generic namemetronidazole
Dosage formTABLET
RouteORAL
Active ingredient(s)METRONIDAZOLE
Strength250 mg/1
Pharmacologic classNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
Marketing categoryANDA

Packages

70518-3042-2 — 28 TABLET in 1 BLISTER PACK (70518-3042-2)

70518-3042-3 — 28 TABLET in 1 BOTTLE, PLASTIC (70518-3042-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69292-208 — metronidazole, 70518-0013 — Metronidazole, 70518-0058 — Metronidazole, 70518-0088 — Metronidazole, 70518-1240 — Metronidazole, 70518-1241 — Metronidazole, 70518-1536 — Metronidazole, 70518-2305 — Metronidazole, 70518-2663 — metronidazole, 70518-2814 — metronidazole, 70518-3110 — Metronidazole, 70518-3265 — 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, +161 more

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