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
70771-1827_859b8e26-b64c-4d17-adbf-0251745c0510
Product NDC
70771-1827
Form
TABLET
Composition / generic term
acetaZOLAMIDE
Labeler
Zydus Lifesciences Limited
Marketing category
ANDA
Marketing start / end (source format)
20230715
Source listing expiry
20261231

Source-listed ingredients

  • ACETAZOLAMIDE — 125 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (70771-1827-1) · 70771-1827-1

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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