Package 70518-4471-0

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4471-0
Digits Only 7051844710
Product NDC 70518-4471
Product ID 70518-4471_3e5df9b1-1506-1ebd-e063-6294a90a12ab
Description

30 TABLET in 1 BLISTER PACK (70518-4471-0)

Marketing

Marketing Status
Marketed Since 2025-09-09
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": "3e5df9b1-1506-1ebd-e063-6294a90a12ab", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["554c7446-8407-460e-b157-f860c5afbf12"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4471-0)", "package_ndc": "70518-4471-0", "marketing_start_date": "20250909"}], "brand_name": "Propranolol Hydrochloride", "product_id": "70518-4471_3e5df9b1-1506-1ebd-e063-6294a90a12ab", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4471", "generic_name": "Propranolol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078955", "marketing_category": "ANDA", "marketing_start_date": "20250909", "listing_expiration_date": "20261231"}