United States · FDA National Drug Code directory

Tindazole

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
64980-427_8dbd79dd-9243-4413-aa01-ba1301573a48
Product NDC
64980-427
Form
TABLET, FILM COATED
Composition / generic term
Tinidazole
Labeler
Rising Pharma Holdings, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20131009
Source listing expiry
20261231

Source-listed ingredients

  • TINIDAZOLE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64980-427-12) · 64980-427-12

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.

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Tindazole — United States | Molindra Medicines