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
- 39822-0190_36974f91-0025-447d-e063-6294a90a0dc2
- Product NDC
- 39822-0190
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Acetazolamide
- Labeler
- XGen Pharmaceuticals DJB, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20081210
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAZOLAMIDE SODIUM — 500 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (39822-0190-1) / 5 mL in 1 VIAL, GLASS · 39822-0190-1
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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