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
- 72162-2678_61ab1dc6-b923-4058-8b85-58a72c9b66ef
- Product NDC
- 72162-2678
- Form
- TABLET, FILM COATED
- Composition / generic term
- Metronidazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260619
- Source listing expiry
- 20271231
Source-listed ingredients
- METRONIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (72162-2678-1) · 72162-2678-1
- 50 TABLET, FILM COATED in 1 BOTTLE (72162-2678-2) · 72162-2678-2
- 500 TABLET, FILM COATED in 1 BOTTLE (72162-2678-5) · 72162-2678-5
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 →