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Metronidazole

NDC 16571-665 · Rising Pharma Holdings, Inc.

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

Packages

16571-665-01 — 100 TABLET in 1 BOTTLE (16571-665-01)

16571-665-50 — 500 TABLET in 1 BOTTLE (16571-665-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0642-7466 — metronidazole, 0713-0574 — metronidazole, 0713-0575 — metronidazole, 0713-0633 — Metronidazole, 0713-0637 — Metronidazole, 0904-7126 — METRONIDAZOLE, 0904-7156 — METRONIDAZOLE, 15955-388 — Metronidazole, 15955-389 — Metronidazole, 16571-664 — Metronidazole, 16714-557 — Metronidazole, 21922-039 — Metronidazole, 21922-046 — Metronidazole vaginal gel, 1.3 %, 21922-070 — Metronidazole Topical, 23155-651 — METRONIDAZOLE, 23155-652 — METRONIDAZOLE, 25021-131 — Metronidazole, 29300-226 — Metronidazole, 29300-227 — Metronidazole, 43063-719 — 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.