Package 63629-2053-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2053-1
Digits Only 6362920531
Product NDC 63629-2053
Product ID 63629-2053_887d805b-d3d6-4b36-aa21-992df0c0201d
Description

500 TABLET, FILM COATED in 1 BOTTLE (63629-2053-1)

Marketing

Marketing Status
Marketed Since 2021-02-02
Brand labetalol hydrochloride
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Labetalol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "887d805b-d3d6-4b36-aa21-992df0c0201d", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896762"], "spl_set_id": ["d073b03d-057d-44eb-a3a7-8f439b965c8a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63629-2053-1)", "package_ndc": "63629-2053-1", "marketing_start_date": "20210202"}], "brand_name": "Labetalol Hydrochloride", "product_id": "63629-2053_887d805b-d3d6-4b36-aa21-992df0c0201d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-2053", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA207863", "marketing_category": "ANDA", "marketing_start_date": "20190524", "listing_expiration_date": "20261231"}