Metronidazole

NDC 72789-005 · PD-Rx Pharmaceuticals, Inc.

Generic nameMetronidazole

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)METRONIDAZOLE

Strength500 mg/1

Pharmacologic classNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]

Marketing categoryANDA

Packages

72789-005-14 — 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-005-14)

FDA lists these products with the same active ingredient.

72162-2259 — Metronidazole, 72162-2403 — Metronidazole, 72162-2468 — metronidazole, 72162-2677 — Metronidazole, 72162-2678 — Metronidazole, 72572-540 — Metronidazole, 72578-007 — metronidazole, 72578-008 — metronidazole, 72578-129 — Metronidazole, 72578-209 — Metronidazole, 72789-007 — Metronidazole, 72789-011 — Metronidazole, 72789-195 — metronidazole, 73473-303 — Metronidazole, 76420-800 — metronidazole, 76420-801 — metronidazole, 76986-005 — Mouthwash, 80830-2465 — Metronidazole, 81033-066 — Metronidazole Oral, 82868-014 — metronidazole, +161 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.