NDC 71335-2372 – Propranolol Hydrochloride

Propranolol Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2372

Product details

Brand name
Propranolol Hydrochloride
Generic name
Propranolol Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071972
Marketed since
June 3, 2021
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-2372-130 TABLET in 1 BOTTLE (71335-2372-1)May 29, 2024
71335-2372-260 TABLET in 1 BOTTLE (71335-2372-2)May 29, 2024
71335-2372-3100 TABLET in 1 BOTTLE (71335-2372-3)May 29, 2024
71335-2372-490 TABLET in 1 BOTTLE (71335-2372-4)May 29, 2024
71335-2372-5120 TABLET in 1 BOTTLE (71335-2372-5)May 29, 2024
71335-2372-610 TABLET in 1 BOTTLE (71335-2372-6)May 29, 2024

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