Package 72888-121-01

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72888-121-01
Digits Only 7288812101
Product NDC 72888-121
Product ID 72888-121_473c8757-9bbe-0aa1-e063-6394a90af1ee
Description

100 TABLET, FILM COATED in 1 BOTTLE (72888-121-01)

Marketing

Marketing Status
Marketed Since 2021-08-18
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": "473c8757-9bbe-0aa1-e063-6394a90af1ee", "openfda": {"upc": ["0372888120010", "0372888120058", "0372888121055", "0372888122014", "0372888122052", "0372888121017"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["1c680447-b43a-4ff1-bc64-2c2174ca1c9a"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72888-121-01)", "package_ndc": "72888-121-01", "marketing_start_date": "20210818"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72888-121-05)", "package_ndc": "72888-121-05", "marketing_start_date": "20210818"}], "brand_name": "LABETALOL HYDROCHLORIDE", "product_id": "72888-121_473c8757-9bbe-0aa1-e063-6394a90af1ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72888-121", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LABETALOL HYDROCHLORIDE", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA211953", "marketing_category": "ANDA", "marketing_start_date": "20210818", "listing_expiration_date": "20261231"}