Package 63629-2070-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2070-1
Digits Only 6362920701
Product NDC 63629-2070
Product ID 63629-2070_d2b77af3-f4da-441d-9eb5-ff1865ade1fa
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2070-1)

Marketing

Marketing Status
Marketed Since 2021-01-28
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": "d2b77af3-f4da-441d-9eb5-ff1865ade1fa", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856481"], "spl_set_id": ["44a7900c-b240-4e04-954e-2671d4d51ae7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2070-1)", "package_ndc": "63629-2070-1", "marketing_start_date": "20210128"}], "brand_name": "propranolol hydrochloride", "product_id": "63629-2070_d2b77af3-f4da-441d-9eb5-ff1865ade1fa", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-2070", "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": "160 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}