Package 63629-2282-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2282-1
Digits Only 6362922821
Product NDC 63629-2282
Product ID 63629-2282_f1f0ae1e-c617-44f2-a18b-418c1198bca4
Description

500 TABLET in 1 BOTTLE (63629-2282-1)

Marketing

Marketing Status
Marketed Since 2010-06-21
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": "f1f0ae1e-c617-44f2-a18b-418c1198bca4", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856578"], "spl_set_id": ["fce3539f-82f3-4bb5-a6ba-c38171c67c06"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-2282-1)", "package_ndc": "63629-2282-1", "marketing_start_date": "20100621"}], "brand_name": "Propranolol Hydrochloride", "product_id": "63629-2282_f1f0ae1e-c617-44f2-a18b-418c1198bca4", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-2282", "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": "80 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}