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
- 62332-016_d9dfe831-5b39-4e51-bf18-3846c3469888
- Product NDC
- 62332-016
- Form
- TABLET
- Composition / generic term
- Metronidazole
- Labeler
- Alembic Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161201
- Source listing expiry
- 20261231
Source-listed ingredients
- METRONIDAZOLE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (62332-016-30) · 62332-016-30
- 100 TABLET in 1 BOTTLE (62332-016-31) · 62332-016-31
- 50 TABLET in 1 BOTTLE (62332-016-50) · 62332-016-50
- 250 TABLET in 1 BOTTLE (62332-016-61) · 62332-016-61
- 500 TABLET in 1 BOTTLE (62332-016-71) · 62332-016-71
- 1000 TABLET in 1 BOTTLE (62332-016-91) · 62332-016-91
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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