Package 0143-9358-01

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0143-9358-01
Digits Only 0143935801
Product NDC 0143-9358
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (0143-9358-01)

Marketing

Marketing Status
Marketed Since 2018-10-15
Brand vancomycin hydrochloride
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fcd91c44-1388-4e34-8078-678c1a640c9c", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["cae9e5f3-b89a-4a7f-93f7-9471c74a3559"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (0143-9358-01)", "package_ndc": "0143-9358-01", "marketing_start_date": "20181015"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "0143-9358_fcd91c44-1388-4e34-8078-678c1a640c9c", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "0143-9358", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "5 g/1"}], "application_number": "ANDA204360", "marketing_category": "ANDA", "marketing_start_date": "20181015", "listing_expiration_date": "20261231"}