Package 50090-7156-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7156-1
Digits Only 5009071561
Product NDC 50090-7156
Product ID 50090-7156_600f7629-8912-496d-872b-753dcdea425a
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-1)

Marketing

Marketing Status
Marketed Since 2024-04-30
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": "600f7629-8912-496d-872b-753dcdea425a", "openfda": {"unii": ["1GEV3BAW9J"], "spl_set_id": ["a007d945-417c-4647-ab03-95ca219d7d38"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-0)", "package_ndc": "50090-7156-0", "marketing_start_date": "20240430"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7156-1)", "package_ndc": "50090-7156-1", "marketing_start_date": "20240430"}], "brand_name": "Labetalol hydrochloride", "product_id": "50090-7156_600f7629-8912-496d-872b-753dcdea425a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7156", "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": "ANDA075133", "marketing_category": "ANDA", "marketing_start_date": "19980803", "listing_expiration_date": "20261231"}