NDC 71335-2781 – Propranolol hydrochloride

Propranolol Hydrochloride 120 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2781

Product details

Brand name
Propranolol hydrochloride
Generic name
Propranolol hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078703
Marketed since
March 11, 2013
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Propranolol Hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
71335-2781-130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2781-1)Oct 13, 2025
71335-2781-260 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2781-2)Oct 13, 2025
71335-2781-3180 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2781-3)Oct 13, 2025
71335-2781-418 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2781-4)Oct 13, 2025
71335-2781-590 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2781-5)Oct 13, 2025

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