NDC 71335-3097 – Propranolol Hydrochloride

Propranolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3097

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
71335-3097-120 TABLET in 1 BOTTLE (71335-3097-1)Mar 13, 2026
71335-3097-230 TABLET in 1 BOTTLE (71335-3097-2)Mar 13, 2026
71335-3097-3100 TABLET in 1 BOTTLE (71335-3097-3)Mar 13, 2026
71335-3097-460 TABLET in 1 BOTTLE (71335-3097-4)Mar 13, 2026
71335-3097-590 TABLET in 1 BOTTLE (71335-3097-5)Mar 13, 2026
71335-3097-6180 TABLET in 1 BOTTLE (71335-3097-6)Mar 13, 2026
71335-3097-728 TABLET in 1 BOTTLE (71335-3097-7)Mar 13, 2026
71335-3097-810 TABLET in 1 BOTTLE (71335-3097-8)Mar 13, 2026
71335-3097-9120 TABLET in 1 BOTTLE (71335-3097-9)Mar 13, 2026

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