NDC 71335-0234 – Propranolol hydrochloride

Propranolol Hydrochloride 60 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC71335-0234

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 (7)

Package NDCDescriptionSince
71335-0234-130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0234-1)Feb 16, 2018
71335-0234-218 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0234-2)Dec 27, 2021
71335-0234-390 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0234-3)Dec 27, 2021
71335-0234-428 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0234-4)Dec 27, 2021
71335-0234-560 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0234-5)Dec 27, 2021
71335-0234-610 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0234-6)Dec 27, 2021
71335-0234-7100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0234-7)Dec 27, 2021

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