Package 0143-9320-01

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9320-01
Digits Only 0143932001
Product NDC 0143-9320
Product ID 0143-9320_cedccb37-4357-4667-bfbf-3208221705c9
Description

1 VIAL in 1 BOX, UNIT-DOSE (0143-9320-01) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 1999-11-29
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": "cedccb37-4357-4667-bfbf-3208221705c9", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896771"], "spl_set_id": ["5b059ef2-dec0-4cea-b8df-d87df3fea9e2"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (0143-9320-01)  / 20 mL in 1 VIAL", "package_ndc": "0143-9320-01", "marketing_start_date": "19991129"}], "brand_name": "Labetalol Hydrochloride", "product_id": "0143-9320_cedccb37-4357-4667-bfbf-3208221705c9", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0143-9320", "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": "ANDA075303", "marketing_category": "ANDA", "marketing_start_date": "19991129", "listing_expiration_date": "20261231"}