Package 63323-284-21
Brand: vancomycin hydrochloride
Generic: vancomycin hydrochloridePackage Facts
Identity
Package NDC
63323-284-21
Digits Only
6332328421
Product NDC
63323-284
Description
10 VIAL in 1 TRAY (63323-284-21) / 20 mL in 1 VIAL
Marketing
Marketing Status
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": "f9a5db80-2985-406e-a7b8-5593e3e8696e", "openfda": {"unii": ["71WO621TJD"], "rxcui": ["1807513"], "spl_set_id": ["83ea3faf-fedd-4725-911f-d71a23ec5d5e"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (63323-284-21) / 20 mL in 1 VIAL", "package_ndc": "63323-284-21", "marketing_start_date": "20000920"}], "brand_name": "VANCOMYCIN HYDROCHLORIDE", "product_id": "63323-284_f9a5db80-2985-406e-a7b8-5593e3e8696e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Glycopeptide Antibacterial [EPC]", "Glycopeptides [CS]"], "product_ndc": "63323-284", "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": "1 g/20mL"}], "application_number": "ANDA062663", "marketing_category": "ANDA", "marketing_start_date": "20000920", "listing_expiration_date": "20261231"}