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
- 44523-450_44ecbffa-e4aa-9dd3-e063-6394a90a4d48
- Product NDC
- 44523-450
- Form
- TABLET, FILM COATED
- Composition / generic term
- tinidazole
- Labeler
- BioComp Pharma, Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20250320
- Source listing expiry
- 20261231
Source-listed ingredients
- TINIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 TABLET, FILM COATED in 1 BOTTLE (44523-450-12) · 44523-450-12
- 20 TABLET, FILM COATED in 1 BOTTLE (44523-450-20) · 44523-450-20
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →