Package 70518-3466-2

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3466-2
Digits Only 7051834662
Product NDC 70518-3466
Product ID 70518-3466_3f0266c8-491e-9a59-e063-6394a90a1a2c
Description

30 TABLET in 1 BLISTER PACK (70518-3466-2)

Marketing

Marketing Status
Marketed Since 2022-10-24
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": "3f0266c8-491e-9a59-e063-6394a90a1a2c", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["a3bd3ef9-539d-450e-900b-95be0e46095b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3466-2)", "package_ndc": "70518-3466-2", "marketing_start_date": "20221024"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3466-3)", "package_ndc": "70518-3466-3", "marketing_start_date": "20240131"}], "brand_name": "Propranolol Hydrochloride", "product_id": "70518-3466_3f0266c8-491e-9a59-e063-6394a90a1a2c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3466", "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": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20220803", "listing_expiration_date": "20261231"}