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
71335-0358_8bc02400-bfe9-4bf1-93b4-f5d287812a8c
Product NDC
71335-0358
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

  • 40 TABLET, FILM COATED in 1 BOTTLE (71335-0358-0) · 71335-0358-0
  • 20 TABLET, FILM COATED in 1 BOTTLE (71335-0358-1) · 71335-0358-1
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0358-2) · 71335-0358-2
  • 14 TABLET, FILM COATED in 1 BOTTLE (71335-0358-3) · 71335-0358-3
  • 56 TABLET, FILM COATED in 1 BOTTLE (71335-0358-4) · 71335-0358-4
  • 21 TABLET, FILM COATED in 1 BOTTLE (71335-0358-5) · 71335-0358-5
  • 4 TABLET, FILM COATED in 1 BOTTLE (71335-0358-6) · 71335-0358-6
  • 28 TABLET, FILM COATED in 1 BOTTLE (71335-0358-7) · 71335-0358-7
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-0358-8) · 71335-0358-8
  • 42 TABLET, FILM COATED in 1 BOTTLE (71335-0358-9) · 71335-0358-9

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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