Package 70518-4454-0

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4454-0
Digits Only 7051844540
Product NDC 70518-4454
Product ID 70518-4454_3d302964-3563-a581-e063-6394a90a7954
Description

30 TABLET in 1 BOTTLE, PLASTIC (70518-4454-0)

Marketing

Marketing Status
Marketed Since 2025-08-22
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Propranolol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3d302964-3563-a581-e063-6394a90a7954", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["9390cfd6-b2e0-48ad-8c4d-ed63cf6b923a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-4454-0)", "package_ndc": "70518-4454-0", "marketing_start_date": "20250822"}], "brand_name": "Propranolol Hydrochloride", "product_id": "70518-4454_3d302964-3563-a581-e063-6394a90a7954", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4454", "generic_name": "Propranolol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078955", "marketing_category": "ANDA", "marketing_start_date": "20250822", "listing_expiration_date": "20261231"}