United States · FDA National Drug Code directory

ACETAZOLAMIDE

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
52817-201_1df8bd81-54fe-44ea-98aa-5f13592dd8bd
Product NDC
52817-201
Form
TABLET
Composition / generic term
ACETAZOLAMIDE
Labeler
TRUPHARMA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20210419
Source listing expiry
20261231

Source-listed ingredients

  • ACETAZOLAMIDE — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE, PLASTIC (52817-201-00) · 52817-201-00
  • 100 TABLET in 1 BOTTLE, PLASTIC (52817-201-10) · 52817-201-10

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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