Package 0615-8426-39

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8426-39
Digits Only 0615842639
Product NDC 0615-8426
Description

30 TABLET in 1 BLISTER PACK (0615-8426-39)

Marketing

Marketing Status
Marketed Since 2022-02-07
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aeffccf0-980b-4e63-a3fb-edcb97995089", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["4d24ea79-ba56-44f4-b1a6-e27235176c4a"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8426-39)", "package_ndc": "0615-8426-39", "marketing_start_date": "20220207"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0615-8426_aeffccf0-980b-4e63-a3fb-edcb97995089", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0615-8426", "generic_name": "Propranolol Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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": "20210603", "listing_expiration_date": "20261231"}