Package 63629-1164-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1164-1
Digits Only 6362911641
Product NDC 63629-1164
Product ID 63629-1164_ac69cf8b-64ca-4e4f-a6af-41c25fd839d8
Description

500 TABLET, FILM COATED in 1 BOTTLE (63629-1164-1)

Marketing

Marketing Status
Marketed Since 2020-10-02
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": "ac69cf8b-64ca-4e4f-a6af-41c25fd839d8", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["R5H8897N95"], "rxcui": ["896762"], "spl_set_id": ["64cd636d-8b48-4f29-b41d-4a048335793e"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63629-1164-1)", "package_ndc": "63629-1164-1", "marketing_start_date": "20201002"}], "brand_name": "Labetalol Hydrochloride", "product_id": "63629-1164_ac69cf8b-64ca-4e4f-a6af-41c25fd839d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-1164", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL", "strength": "200 mg/1"}], "application_number": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20191122", "listing_expiration_date": "20261231"}