Package 70518-4292-0

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4292-0
Digits Only 7051842920
Product NDC 70518-4292
Product ID 70518-4292_401c0113-427e-ed32-e063-6294a90a3e2b
Description

30 TABLET in 1 BLISTER PACK (70518-4292-0)

Marketing

Marketing Status
Marketed Since 2025-02-25
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": "401c0113-427e-ed32-e063-6294a90a3e2b", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["f7ae2dac-6048-41ea-95d3-cad06cc2baf3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4292-0)", "package_ndc": "70518-4292-0", "marketing_start_date": "20250225"}], "brand_name": "Propranolol Hydrochloride", "product_id": "70518-4292_401c0113-427e-ed32-e063-6294a90a3e2b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4292", "generic_name": "Propranolol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20250225", "listing_expiration_date": "20261231"}