Package 50090-6833-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6833-1
Digits Only 5009068331
Product NDC 50090-6833
Product ID 50090-6833_7615303f-6f49-4281-bf0d-5c49bbaa7ae2
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6833-1)

Marketing

Marketing Status
Marketed Since 2023-11-21
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": "7615303f-6f49-4281-bf0d-5c49bbaa7ae2", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896766"], "spl_set_id": ["5faacbcc-f88f-42f7-8702-791ee82c4d18"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6833-1)", "package_ndc": "50090-6833-1", "marketing_start_date": "20231121"}], "brand_name": "Labetalol Hydrochloride", "product_id": "50090-6833_7615303f-6f49-4281-bf0d-5c49bbaa7ae2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-6833", "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": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20210208", "listing_expiration_date": "20261231"}