Package 55150-205-99

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55150-205-99
Digits Only 5515020599
Product NDC 55150-205
Product ID 55150-205_a5a491c0-5875-4031-b547-c33e02413357
Description

1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-205-99) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE

Marketing

Marketing Status
Marketed Since 2016-03-29
Brand vancomycin hydrochloride
Generic vancomycin hydrochloride
Sample Package No

Linked Drug Pages (1)

Vancomycin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "a5a491c0-5875-4031-b547-c33e02413357", "openfda": {"upc": ["0355150206995", "0355150205998"], "unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["4a80cb3f-7410-47aa-af1f-ff83d1b35c55"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-205-99)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "55150-205-99", "marketing_start_date": "20160329"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "55150-205_a5a491c0-5875-4031-b547-c33e02413357", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "55150-205", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "5 g/1"}], "application_number": "ANDA205779", "marketing_category": "ANDA", "marketing_start_date": "20160329", "listing_expiration_date": "20261231"}