Package 55154-0182-0

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-0182-0
Digits Only 5515401820
Product NDC 55154-0182
Product ID 55154-0182_6054fdc7-f467-40f7-9ffe-92e20736ffbf
Description

10 BLISTER PACK in 1 BAG (55154-0182-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-05-06
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": "6054fdc7-f467-40f7-9ffe-92e20736ffbf", "openfda": {"upc": ["0055154018104", "0055154018401", "0055154018203"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["d3ca153c-25b2-4506-91bd-bf9d6a4c01fe"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-0182-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-0182-0", "marketing_start_date": "20250506"}], "brand_name": "Labetalol Hydrochloride", "product_id": "55154-0182_6054fdc7-f467-40f7-9ffe-92e20736ffbf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "55154-0182", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA209603", "marketing_category": "ANDA", "marketing_start_date": "20250506", "listing_expiration_date": "20271231"}