Package 72572-350-01

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72572-350-01
Digits Only 7257235001
Product NDC 72572-350
Product ID 72572-350_076e0f01-e1cb-4948-9d90-865ff7d4a47c
Description

1 VIAL in 1 BOX, UNIT-DOSE (72572-350-01) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2019-11-21
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": ["INTRAVENOUS"], "spl_id": "076e0f01-e1cb-4948-9d90-865ff7d4a47c", "openfda": {"upc": ["0372572350013"], "unii": ["1GEV3BAW9J"], "rxcui": ["896771"], "spl_set_id": ["d7c53b1c-b6a5-482a-a7c8-7425d9cd9ef8"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (72572-350-01)  / 20 mL in 1 VIAL", "package_ndc": "72572-350-01", "marketing_start_date": "20191121"}], "brand_name": "Labetalol Hydrochloride", "product_id": "72572-350_076e0f01-e1cb-4948-9d90-865ff7d4a47c", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72572-350", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA075303", "marketing_category": "ANDA", "marketing_start_date": "20191121", "listing_expiration_date": "20261231"}