Package 72888-468-02

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72888-468-02
Digits Only 7288846802
Product NDC 72888-468
Product ID 72888-468_35a89027-9232-dad9-e063-6394a90a7787
Description

100 TABLET, FILM COATED in 1 BOTTLE (72888-468-02)

Marketing

Marketing Status
Marketed Since 2025-05-20
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": "35a89027-9232-dad9-e063-6394a90a7787", "openfda": {"upc": ["0372888468020", "0372888468013"], "unii": ["1GEV3BAW9J"], "rxcui": ["896766"], "spl_set_id": ["106a0959-5830-489f-ba60-afd4eb0fac36"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72888-468-01)", "package_ndc": "72888-468-01", "marketing_start_date": "20250520"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72888-468-02)", "package_ndc": "72888-468-02", "marketing_start_date": "20250520"}], "brand_name": "LABETALOL HYDROCHLORIDE", "product_id": "72888-468_35a89027-9232-dad9-e063-6394a90a7787", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72888-468", "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": "300 mg/1"}], "application_number": "ANDA211953", "marketing_category": "ANDA", "marketing_start_date": "20250520", "listing_expiration_date": "20261231"}