Package 63323-314-66

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-314-66
Digits Only 6332331466
Product NDC 63323-314
Description

1 BOTTLE in 1 CARTON (63323-314-66) / 100 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2004-11-30
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": "020618ad-8f1f-4189-a95c-254f05a077cc", "openfda": {"upc": ["0363323295660", "0363323314668"], "unii": ["71WO621TJD"], "rxcui": ["239209", "313572"], "spl_set_id": ["0713a847-a334-4b73-af22-343aa06621b9"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63323-314-66)  / 100 mL in 1 BOTTLE", "package_ndc": "63323-314-66", "marketing_start_date": "20041130"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "63323-314_020618ad-8f1f-4189-a95c-254f05a077cc", "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 USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vancomycin Hydrochloride", "active_ingredients": [{"name": "VANCOMYCIN HYDROCHLORIDE", "strength": "10 g/100mL"}], "application_number": "ANDA062663", "marketing_category": "ANDA", "marketing_start_date": "20041130", "listing_expiration_date": "20261231"}