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
- 47335-993_53cfb044-6f56-f028-e063-6394a90a53f2
- Product NDC
- 47335-993
- Form
- INJECTION, SOLUTION
- Composition / generic term
- metronidazole
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210810
- Source listing expiry
- 20271231
Source-listed ingredients
- METRONIDAZOLE — 500 mg/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BAG in 1 POUCH (47335-993-01) / 100 mL in 1 BAG · 47335-993-01
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 →