United States · FDA National Drug Code directory
Sotalol Hydrochloride
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
- 0904-7143_2b64f084-8d8f-454c-834b-16e8d1439c77
- Product NDC
- 0904-7143
- Form
- TABLET
- Composition / generic term
- Sotalol Hydrochloride
- Labeler
- Major Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20030201
- Source listing expiry
- 20261231
Source-listed ingredients
- SOTALOL HYDROCHLORIDE — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 CARTON (0904-7143-61) / 1 TABLET in 1 BLISTER PACK · 0904-7143-61
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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