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
- 70756-721_be4d7d81-4fe9-4a54-a7c0-18f825eeba98
- Product NDC
- 70756-721
- Form
- TABLET
- Composition / generic term
- Acetazolamide
- Labeler
- Lifestar Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201113
- Source listing expiry
- 20271231
Source-listed ingredients
- ACETAZOLAMIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (70756-721-11) · 70756-721-11
- 10 BLISTER PACK in 1 CARTON (70756-721-99) / 10 TABLET in 1 BLISTER PACK · 70756-721-99
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.
Browse United States records →