NDC 71335-2369 – Propranolol Hydrochloride

Propranolol Hydrochloride 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2369

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 (9)

Package NDCDescriptionSince
71335-2369-130 TABLET in 1 BOTTLE (71335-2369-1)May 23, 2024
71335-2369-260 TABLET in 1 BOTTLE (71335-2369-2)May 23, 2024
71335-2369-390 TABLET in 1 BOTTLE (71335-2369-3)May 23, 2024
71335-2369-4100 TABLET in 1 BOTTLE (71335-2369-4)May 23, 2024
71335-2369-5180 TABLET in 1 BOTTLE (71335-2369-5)May 23, 2024
71335-2369-620 TABLET in 1 BOTTLE (71335-2369-6)May 23, 2024
71335-2369-728 TABLET in 1 BOTTLE (71335-2369-7)May 23, 2024
71335-2369-810 TABLET in 1 BOTTLE (71335-2369-8)May 23, 2024
71335-2369-9120 TABLET in 1 BOTTLE (71335-2369-9)May 23, 2024

Other Propranolol Hydrochloride products