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
- 63629-7916_1d6e2095-0b00-4773-ac12-06c7aef3ecc5
- Product NDC
- 63629-7916
- Form
- TABLET, FILM COATED
- Composition / generic term
- Metronidazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140601
- Source listing expiry
- 20261231
Source-listed ingredients
- METRONIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET, FILM COATED in 1 BOTTLE (63629-7916-1) · 63629-7916-1
- 3 TABLET, FILM COATED in 1 BOTTLE (63629-7916-2) · 63629-7916-2
- 9 TABLET, FILM COATED in 1 BOTTLE (63629-7916-3) · 63629-7916-3
- 10 TABLET, FILM COATED in 1 BOTTLE (63629-7916-4) · 63629-7916-4
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 →