Package 63629-2072-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2072-1
Digits Only 6362920721
Product NDC 63629-2072
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2072-1)

Marketing

Marketing Status
Marketed Since 2021-01-28
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": "011d97be-9c97-412c-85e3-f877890e40f3", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["5ee3776f-9d02-4d98-bc9d-e810c87961c3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2072-1)", "package_ndc": "63629-2072-1", "marketing_start_date": "20210128"}], "brand_name": "propranolol hydrochloride", "product_id": "63629-2072_011d97be-9c97-412c-85e3-f877890e40f3", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-2072", "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": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}