Package 63629-2071-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2071-1
Digits Only 6362920711
Product NDC 63629-2071
Product ID 63629-2071_16056bc7-61f0-43a5-9c1f-42bff647b230
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2071-1)

Marketing

Marketing Status
Marketed Since 2013-03-11
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": "16056bc7-61f0-43a5-9c1f-42bff647b230", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856535"], "spl_set_id": ["8e675a00-2b20-4fcd-baa0-661bcf9809c8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2071-1)", "package_ndc": "63629-2071-1", "marketing_start_date": "20130311"}], "brand_name": "propranolol hydrochloride", "product_id": "63629-2071_16056bc7-61f0-43a5-9c1f-42bff647b230", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-2071", "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": "60 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}