Package 0409-2339-34

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-2339-34
Digits Only 0409233934
Product NDC 0409-2339
Description

10 CARTON in 1 PACKAGE (0409-2339-34) / 1 CARTRIDGE in 1 CARTON / 4 mL in 1 CARTRIDGE (0409-2339-24)

Marketing

Marketing Status
Marketed Since 2005-10-18
Brand labetalol hydrochloride
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "7ba44762-b760-4a8f-adce-65bf78cc5d98", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["1234256"], "spl_set_id": ["d3579d45-a964-40fe-e3a2-a3a997c8b7b9"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 PACKAGE (0409-2339-34)  / 1 CARTRIDGE in 1 CARTON / 4 mL in 1 CARTRIDGE (0409-2339-24)", "package_ndc": "0409-2339-34", "marketing_start_date": "20051018"}], "brand_name": "Labetalol Hydrochloride", "product_id": "0409-2339_7ba44762-b760-4a8f-adce-65bf78cc5d98", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0409-2339", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA075239", "marketing_category": "ANDA", "marketing_start_date": "20051018", "listing_expiration_date": "20261231"}