Package 70518-3377-0

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3377-0
Digits Only 7051833770
Product NDC 70518-3377
Product ID 70518-3377_3a757b47-86b8-a0ad-e063-6294a90a0da6
Description

30 TABLET in 1 BLISTER PACK (70518-3377-0)

Marketing

Marketing Status
Marketed Since 2022-03-06
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": "3a757b47-86b8-a0ad-e063-6294a90a0da6", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["e3f615e0-07da-491c-9620-7083f4f4318a"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3377-0)", "package_ndc": "70518-3377-0", "marketing_start_date": "20220306"}], "brand_name": "Propranolol Hydrochloride", "product_id": "70518-3377_3a757b47-86b8-a0ad-e063-6294a90a0da6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3377", "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": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20220306", "listing_expiration_date": "20261231"}