Package 51407-615-05

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51407-615-05
Digits Only 5140761505
Product NDC 51407-615
Description

500 TABLET, FILM COATED in 1 BOTTLE (51407-615-05)

Marketing

Marketing Status
Marketed Since 2021-12-03
Brand labetalol hydrochloride
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "411092bf-427f-2d66-e063-6294a90a2ccb", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["d5ce687f-4a37-d3e6-e053-2995a90aa974"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (51407-615-01)", "package_ndc": "51407-615-01", "marketing_start_date": "20211203"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (51407-615-05)", "package_ndc": "51407-615-05", "marketing_start_date": "20211203"}], "brand_name": "Labetalol Hydrochloride", "product_id": "51407-615_411092bf-427f-2d66-e063-6294a90a2ccb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51407-615", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "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": "20180620", "listing_expiration_date": "20261231"}