Package 63323-221-48

Brand: vancomycin hydrochloride

Generic: vancomycin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-221-48
Digits Only 6332322148
Product NDC 63323-221
Product ID 63323-221_23a89459-d331-4975-84fe-4bfa6ed2c24e
Description

25 VIAL in 1 TRAY (63323-221-48) / 10 mL in 1 VIAL (63323-221-43)

Marketing

Marketing Status
Marketed Since 2017-10-26
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": "23a89459-d331-4975-84fe-4bfa6ed2c24e", "openfda": {"upc": ["0363323284411", "0363323221430"], "unii": ["71WO621TJD"], "rxcui": ["1807513", "1807516"], "spl_set_id": ["418c3c6a-d08d-448c-89c9-54e558c1ce16"], "manufacturer_name": ["Fresenius Kabi, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (63323-221-48)  / 10 mL in 1 VIAL (63323-221-43)", "package_ndc": "63323-221-48", "marketing_start_date": "20171026"}], "brand_name": "Vancomycin Hydrochloride", "product_id": "63323-221_23a89459-d331-4975-84fe-4bfa6ed2c24e", "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": "20171026", "listing_expiration_date": "20261231"}