Package 50090-7666-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7666-1
Digits Only 5009076661
Product NDC 50090-7666
Product ID 50090-7666_904fbf22-4fe2-47b4-a2ee-514fb4eed012
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7666-1)

Marketing

Marketing Status
Marketed Since 2025-10-01
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": "904fbf22-4fe2-47b4-a2ee-514fb4eed012", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896766"], "spl_set_id": ["fffb7c59-ad92-4e74-850d-d94d42b7fdc9"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7666-1)", "package_ndc": "50090-7666-1", "marketing_start_date": "20251001"}], "brand_name": "LABETALOL HYDROCHLORIDE", "product_id": "50090-7666_904fbf22-4fe2-47b4-a2ee-514fb4eed012", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7666", "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": "300 mg/1"}], "application_number": "ANDA211953", "marketing_category": "ANDA", "marketing_start_date": "20210818", "listing_expiration_date": "20261231"}