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
- 70710-1591_4ee1e84b-1f11-43bb-8945-e6e302c58685
- Product NDC
- 70710-1591
- Form
- CAPSULE
- Composition / generic term
- acetazolamide
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190508
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAZOLAMIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE in 1 BOTTLE (70710-1591-0) · 70710-1591-0
- 100 CAPSULE in 1 BOTTLE (70710-1591-1) · 70710-1591-1
- 30 CAPSULE in 1 BOTTLE (70710-1591-3) · 70710-1591-3
- 10 BLISTER PACK in 1 CARTON (70710-1591-4) / 10 CAPSULE in 1 BLISTER PACK · 70710-1591-4
- 500 CAPSULE in 1 BOTTLE (70710-1591-5) · 70710-1591-5
- 90 CAPSULE in 1 BOTTLE (70710-1591-9) · 70710-1591-9
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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