NDC 71335-3137 – Propranolol Hydrochloride

Propranolol Hydrochloride 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3137

Product details

Brand name
Propranolol Hydrochloride
Generic name
Propranolol Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078955
Marketed since
September 19, 2024
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-3137-130 TABLET in 1 BOTTLE (71335-3137-1)May 27, 2026
71335-3137-260 TABLET in 1 BOTTLE (71335-3137-2)May 27, 2026
71335-3137-390 TABLET in 1 BOTTLE (71335-3137-3)May 27, 2026
71335-3137-4100 TABLET in 1 BOTTLE (71335-3137-4)May 27, 2026
71335-3137-5180 TABLET in 1 BOTTLE (71335-3137-5)May 27, 2026
71335-3137-620 TABLET in 1 BOTTLE (71335-3137-6)May 27, 2026
71335-3137-728 TABLET in 1 BOTTLE (71335-3137-7)May 27, 2026
71335-3137-810 TABLET in 1 BOTTLE (71335-3137-8)May 27, 2026
71335-3137-9120 TABLET in 1 BOTTLE (71335-3137-9)May 27, 2026

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