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
- 68071-1876_59fbcd33-af2f-503f-e063-6294a90acbb9
- Product NDC
- 68071-1876
- Form
- TABLET, FILM COATED
- Composition / generic term
- Metronidazole
- Labeler
- NuCare Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140601
- Source listing expiry
- 20271231
Source-listed ingredients
- METRONIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 42 TABLET, FILM COATED in 1 BOTTLE (68071-1876-0) · 68071-1876-0
- 4 TABLET, FILM COATED in 1 BOTTLE (68071-1876-1) · 68071-1876-1
- 21 TABLET, FILM COATED in 1 BOTTLE (68071-1876-2) · 68071-1876-2
- 30 TABLET, FILM COATED in 1 BOTTLE (68071-1876-3) · 68071-1876-3
- 14 TABLET, FILM COATED in 1 BOTTLE (68071-1876-4) · 68071-1876-4
- 40 TABLET, FILM COATED in 1 BOTTLE (68071-1876-5) · 68071-1876-5
- 20 TABLET, FILM COATED in 1 BOTTLE (68071-1876-7) · 68071-1876-7
- 28 TABLET, FILM COATED in 1 BOTTLE (68071-1876-8) · 68071-1876-8
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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