Package 71335-1410-1

Brand: labetalol hcl

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1410-1
Digits Only 7133514101
Product NDC 71335-1410
Product ID 71335-1410_98b598e0-64b7-4a8c-9c7f-a8891fd4e708
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-1410-1)

Marketing

Marketing Status
Marketed Since 2024-10-07
Brand labetalol hcl
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Labetalol HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "98b598e0-64b7-4a8c-9c7f-a8891fd4e708", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896766"], "spl_set_id": ["06ff81fe-9226-49a7-aa5c-f52b059d7cab"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1410-1)", "package_ndc": "71335-1410-1", "marketing_start_date": "20241007"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1410-2)", "package_ndc": "71335-1410-2", "marketing_start_date": "20191127"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-1410-3)", "package_ndc": "71335-1410-3", "marketing_start_date": "20241007"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1410-4)", "package_ndc": "71335-1410-4", "marketing_start_date": "20241007"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-1410-5)", "package_ndc": "71335-1410-5", "marketing_start_date": "20241007"}], "brand_name": "Labetalol HCL", "product_id": "71335-1410_98b598e0-64b7-4a8c-9c7f-a8891fd4e708", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-1410", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol HCL", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA200908", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}