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
- 82804-951_10b7b81d-9ce7-4025-8559-fdfa41c8b146
- Product NDC
- 82804-951
- Form
- TABLET
- Composition / generic term
- Sotalol Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200724
- Source listing expiry
- 20271231
Source-listed ingredients
- SOTALOL HYDROCHLORIDE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (82804-951-00) · 82804-951-00
- 1000 TABLET in 1 BOTTLE (82804-951-11) · 82804-951-11
- 30 TABLET in 1 BOTTLE (82804-951-30) · 82804-951-30
- 500 TABLET in 1 BOTTLE (82804-951-55) · 82804-951-55
- 60 TABLET in 1 BOTTLE (82804-951-60) · 82804-951-60
- 120 TABLET in 1 BOTTLE (82804-951-72) · 82804-951-72
- 90 TABLET in 1 BOTTLE (82804-951-90) · 82804-951-90
- 300 TABLET in 1 BOTTLE (82804-951-96) · 82804-951-96
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 →