Package 72603-146-01

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-146-01
Digits Only 7260314601
Product NDC 72603-146
Product ID 72603-146_a2d07ec0-3718-40eb-9d0a-79c557c486b9
Description

1 VIAL, MULTI-DOSE in 1 CARTON (72603-146-01) / 20 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2023-04-28
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": "a2d07ec0-3718-40eb-9d0a-79c557c486b9", "openfda": {"upc": ["0372603146011"], "unii": ["1GEV3BAW9J"], "rxcui": ["896771"], "spl_set_id": ["a2d07ec0-3718-40eb-9d0a-79c557c486b9"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (72603-146-01)  / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "72603-146-01", "marketing_start_date": "20230428"}], "brand_name": "Labetalol Hydrochloride", "product_id": "72603-146_a2d07ec0-3718-40eb-9d0a-79c557c486b9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72603-146", "generic_name": "Labetalol Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA214533", "marketing_category": "ANDA", "marketing_start_date": "20230428", "listing_expiration_date": "20261231"}