NDC 71335-0472 – Propranolol Hydrochloride

Propranolol Hydrochloride 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0472

Product details

Brand name
Propranolol Hydrochloride
Generic name
Propranolol hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070221
Marketed since
June 21, 2010
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-0472-130 TABLET in 1 BOTTLE (71335-0472-1)Oct 7, 2015
71335-0472-260 TABLET in 1 BOTTLE (71335-0472-2)Oct 7, 2015
71335-0472-390 TABLET in 1 BOTTLE (71335-0472-3)Oct 7, 2015
71335-0472-4100 TABLET in 1 BOTTLE (71335-0472-4)Oct 7, 2015
71335-0472-5180 TABLET in 1 BOTTLE (71335-0472-5)Oct 7, 2015
71335-0472-620 TABLET in 1 BOTTLE (71335-0472-6)Oct 7, 2015
71335-0472-728 TABLET in 1 BOTTLE (71335-0472-7)Oct 7, 2015
71335-0472-810 TABLET in 1 BOTTLE (71335-0472-8)Oct 7, 2015
71335-0472-9120 TABLET in 1 BOTTLE (71335-0472-9)Oct 7, 2015

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