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
- 51655-441_4b4409ed-781d-8784-e063-6294a90a580a
- Product NDC
- 51655-441
- Form
- TABLET
- Composition / generic term
- METRONIDAZOLE
- Labeler
- Northwind Health Company, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221130
- Source listing expiry
- 20271231
Source-listed ingredients
- METRONIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE, PLASTIC (51655-441-20) · 51655-441-20
- 21 TABLET in 1 BOTTLE, PLASTIC (51655-441-21) · 51655-441-21
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-441-52) · 51655-441-52
- 14 TABLET in 1 BOTTLE, PLASTIC (51655-441-84) · 51655-441-84
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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