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
- 72789-007_4030e823-df78-74d4-e063-6394a90ac806
- Product NDC
- 72789-007
- Form
- TABLET
- Composition / generic term
- Metronidazole
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161201
- Source listing expiry
- 20261231
Source-listed ingredients
- METRONIDAZOLE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET in 1 BOTTLE, PLASTIC (72789-007-04) · 72789-007-04
- 6 TABLET in 1 BOTTLE, PLASTIC (72789-007-06) · 72789-007-06
- 9 TABLET in 1 BOTTLE, PLASTIC (72789-007-09) · 72789-007-09
- 14 TABLET in 1 BOTTLE, PLASTIC (72789-007-14) · 72789-007-14
- 21 TABLET in 1 BOTTLE, PLASTIC (72789-007-21) · 72789-007-21
- 28 TABLET in 1 BOTTLE, PLASTIC (72789-007-28) · 72789-007-28
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-007-30) · 72789-007-30
- 1 TABLET in 1 BOTTLE, PLASTIC (72789-007-79) · 72789-007-79
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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