Package 63323-321-10
Brand: polymyxin b
Generic: polymyxin b sulfatePackage Facts
Identity
Package NDC
63323-321-10
Digits Only
6332332110
Product NDC
63323-321
Description
10 VIAL in 1 TRAY (63323-321-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (63323-321-01)
Marketing
Marketing Status
Brand
polymyxin b
Generic
polymyxin b sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRATHECAL", "INTRAVENOUS", "OPHTHALMIC"], "spl_id": "545b3d1d-6c8f-44aa-b81e-b24fc99f9c82", "openfda": {"upc": ["0363323321017"], "unii": ["19371312D4"], "rxcui": ["204509"], "spl_set_id": ["fbc12c18-567b-41bc-89d0-efd29616615c"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (63323-321-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (63323-321-01)", "package_ndc": "63323-321-10", "marketing_start_date": "20091117"}], "brand_name": "POLYMYXIN B", "product_id": "63323-321_545b3d1d-6c8f-44aa-b81e-b24fc99f9c82", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "63323-321", "generic_name": "POLYMYXIN B SULFATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POLYMYXIN B", "active_ingredients": [{"name": "POLYMYXIN B SULFATE", "strength": "500000 [USP'U]/1"}], "application_number": "ANDA065372", "marketing_category": "ANDA", "marketing_start_date": "20091117", "listing_expiration_date": "20261231"}