NDC 70518-3466 – Propranolol Hydrochloride

Propranolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-3466

Product details

Brand name
Propranolol Hydrochloride
Generic name
Propranolol Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071972
Marketed since
August 3, 2022
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70518-3466-230 TABLET in 1 BLISTER PACK (70518-3466-2)Oct 24, 2022
70518-3466-330 TABLET in 1 BLISTER PACK (70518-3466-3)Jan 31, 2024

Other Propranolol Hydrochloride products