NDC 0093-1061 – Sotalol Hydrochloride

Sotalol Hydrochloride 80 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-1061

Product details

Brand name
Sotalol Hydrochloride
Generic name
Sotalol Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075429
Marketed since
May 4, 2000
Listing expires
December 31, 2026
Pharmacologic class
Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for Sotalol hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0093-1061-01100 TABLET in 1 BOTTLE (0093-1061-01)May 4, 2000

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