Package 63323-221-38

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-221-38
Digits Only 6332322138
Product NDC 63323-221
Product ID 63323-221_0ab54d7b-de6b-412f-b2b5-a8522f78f3c4
Description

25 VIAL in 1 TRAY (63323-221-38) / 10 mL in 1 VIAL (63323-221-33)

Marketing

Marketing Status
Marketed Since 2017-11-01
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": "0ab54d7b-de6b-412f-b2b5-a8522f78f3c4", "openfda": {"upc": ["0363323221331"], "unii": ["71WO621TJD"], "rxcui": ["1807516"], "spl_set_id": ["8a35ebee-8650-4ef5-84f5-ab9b55d9bc19"], "manufacturer_name": ["Fresenius Kabi, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (63323-221-38)  / 10 mL in 1 VIAL (63323-221-33)", "package_ndc": "63323-221-38", "marketing_start_date": "20171101"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "63323-221_0ab54d7b-de6b-412f-b2b5-a8522f78f3c4", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "63323-221", "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": "500 mg/10mL"}], "application_number": "ANDA204107", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20261231"}