United States · FDA National Drug Code directory
Tinidazole
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
- 43386-551_98a66e10-fb32-46ce-a68b-c21d615f6621
- Product NDC
- 43386-551
- Form
- TABLET
- Composition / generic term
- Tinidazole
- Labeler
- Lupin Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120430
- Source listing expiry
- 20261231
Source-listed ingredients
- TINIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (43386-551-02) · 43386-551-02
- 60 TABLET in 1 BOTTLE (43386-551-06) · 43386-551-06
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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