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
- 68788-7815_1820c0da-b46b-409a-8e06-98acd1189737
- Product NDC
- 68788-7815
- Form
- TABLET
- Composition / generic term
- metronidazole
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201113
- Source listing expiry
- 20271231
Source-listed ingredients
- METRONIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET in 1 BOTTLE (68788-7815-1) · 68788-7815-1
- 21 TABLET in 1 BOTTLE (68788-7815-2) · 68788-7815-2
- 30 TABLET in 1 BOTTLE (68788-7815-3) · 68788-7815-3
- 28 TABLET in 1 BOTTLE (68788-7815-4) · 68788-7815-4
- 56 TABLET in 1 BOTTLE (68788-7815-5) · 68788-7815-5
- 42 TABLET in 1 BOTTLE (68788-7815-7) · 68788-7815-7
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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