Package 63323-314-68

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-314-68
Digits Only 6332331468
Product NDC 63323-314
Description

1 BOTTLE in 1 CARTON (63323-314-68) / 100 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-09-01
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": "d11a86ee-15b0-49cf-880a-f4b3b70e22cf", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["239209"], "spl_set_id": ["a7e7d990-1d74-459b-ac07-d1c3e13b3204"], "manufacturer_name": ["Fresenius Kabi, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63323-314-68)  / 100 mL in 1 BOTTLE", "package_ndc": "63323-314-68", "marketing_start_date": "20170901"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "63323-314_d11a86ee-15b0-49cf-880a-f4b3b70e22cf", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "63323-314", "generic_name": "Vancomycin Hydrochloride", "labeler_name": "Fresenius Kabi, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "10 g/100mL"}], "application_number": "ANDA204125", "marketing_category": "ANDA", "marketing_start_date": "20170901", "listing_expiration_date": "20261231"}