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
- 68071-2409_10f6b5cd-3cf8-e2fe-e063-6394a90a690c
- Product NDC
- 68071-2409
- Form
- TABLET
- Composition / generic term
- metronidazole
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190223
- Source listing expiry
- 20261231
Source-listed ingredients
- METRONIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET in 1 BOTTLE (68071-2409-1) · 68071-2409-1
- 21 TABLET in 1 BOTTLE (68071-2409-2) · 68071-2409-2
- 30 TABLET in 1 BOTTLE (68071-2409-3) · 68071-2409-3
- 14 TABLET in 1 BOTTLE (68071-2409-4) · 68071-2409-4
- 40 TABLET in 1 BOTTLE (68071-2409-5) · 68071-2409-5
- 20 TABLET in 1 BOTTLE (68071-2409-7) · 68071-2409-7
- 28 TABLET in 1 BOTTLE (68071-2409-8) · 68071-2409-8
- 90 TABLET in 1 BOTTLE (68071-2409-9) · 68071-2409-9
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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