Package 50090-7731-0

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7731-0
Digits Only 5009077310
Product NDC 50090-7731
Product ID 50090-7731_8cc0d957-ec60-4a7e-b36b-aab0b4d75d5d
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7731-0)

Marketing

Marketing Status
Marketed Since 2025-10-28
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": "8cc0d957-ec60-4a7e-b36b-aab0b4d75d5d", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896762"], "spl_set_id": ["e6836a01-220d-4b69-9b4a-c919daeb6ece"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7731-0)", "package_ndc": "50090-7731-0", "marketing_start_date": "20251028"}], "brand_name": "LABETALOL HYDROCHLORIDE", "product_id": "50090-7731_8cc0d957-ec60-4a7e-b36b-aab0b4d75d5d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7731", "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": "ANDA211953", "marketing_category": "ANDA", "marketing_start_date": "20210818", "listing_expiration_date": "20261231"}