NDC 71335-2371 – Propranolol Hydrochloride

Propranolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2371

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
71335-2371-120 TABLET in 1 BOTTLE (71335-2371-1)May 23, 2024
71335-2371-230 TABLET in 1 BOTTLE (71335-2371-2)May 23, 2024
71335-2371-3100 TABLET in 1 BOTTLE (71335-2371-3)May 23, 2024
71335-2371-460 TABLET in 1 BOTTLE (71335-2371-4)May 23, 2024
71335-2371-590 TABLET in 1 BOTTLE (71335-2371-5)May 23, 2024
71335-2371-6180 TABLET in 1 BOTTLE (71335-2371-6)May 23, 2024
71335-2371-728 TABLET in 1 BOTTLE (71335-2371-7)May 23, 2024
71335-2371-810 TABLET in 1 BOTTLE (71335-2371-8)May 23, 2024
71335-2371-9120 TABLET in 1 BOTTLE (71335-2371-9)May 23, 2024

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