Package 0143-9183-10

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9183-10
Digits Only 0143918310
Product NDC 0143-9183
Description

10 VIAL in 1 CARTON (0143-9183-10) / 4 mL in 1 VIAL (0143-9183-01)

Marketing

Marketing Status
Marketed Since 2025-08-28
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": "d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["2477889", "2479564", "2479566", "2479567"], "spl_set_id": ["99a715a0-4579-410c-b102-7ef6fab8db55"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9183-10)  / 4 mL in 1 VIAL (0143-9183-01)", "package_ndc": "0143-9183-10", "marketing_start_date": "20250828"}], "brand_name": "Labetalol Hydrochloride", "product_id": "0143-9183_d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0143-9183", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "NDA213330", "marketing_category": "NDA", "marketing_start_date": "20250828", "listing_expiration_date": "20261231"}