Package 63629-2279-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2279-1
Digits Only 6362922791
Product NDC 63629-2279
Description

1000 TABLET in 1 BOTTLE (63629-2279-1)

Marketing

Marketing Status
Marketed Since 2010-06-21
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": "25017b59-96d7-4cf6-90d6-4d46fb449f57", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["b27ade81-8b41-4394-aec1-d23370bfa3b7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-2279-1)", "package_ndc": "63629-2279-1", "marketing_start_date": "20100621"}], "brand_name": "Propranolol Hydrochloride", "product_id": "63629-2279_25017b59-96d7-4cf6-90d6-4d46fb449f57", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-2279", "generic_name": "propranolol hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}