United States · FDA National Drug Code directory
Metronidazole
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 23155-651_a144e3b5-1edf-446a-99cd-51f4f8ce8dc5
- Product NDC
- 23155-651
- Form
- TABLET
- Composition / generic term
- METRONIDAZOLE
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171129
- Source listing expiry
- 20261231
Source-listed ingredients
- METRONIDAZOLE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (23155-651-01) · 23155-651-01
- 500 TABLET in 1 BOTTLE, PLASTIC (23155-651-05) · 23155-651-05
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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