Package 50090-7524-0

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7524-0
Digits Only 5009075240
Product NDC 50090-7524
Product ID 50090-7524_eac89f67-1d17-42e0-a8d8-1cbe0dec9cbf
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7524-0)

Marketing

Marketing Status
Marketed Since 2025-03-18
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": "eac89f67-1d17-42e0-a8d8-1cbe0dec9cbf", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896762"], "spl_set_id": ["f9af85d3-a5a7-49d6-aff6-1ca2b2d75450"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7524-0)", "package_ndc": "50090-7524-0", "marketing_start_date": "20250318"}], "brand_name": "Labetalol Hydrochloride", "product_id": "50090-7524_eac89f67-1d17-42e0-a8d8-1cbe0dec9cbf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7524", "generic_name": "Labetalol Hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20210527", "listing_expiration_date": "20271231"}