Package 63323-321-12

Brand: polymyxin b

Generic: polymyxin b sulfate
NDC Package

Package Facts

Identity

Package NDC 63323-321-12
Digits Only 6332332112
Product NDC 63323-321
Product ID 63323-321_b473292e-e7ce-4ce2-aec7-91604b82bb11
Description

10 VIAL in 1 TRAY (63323-321-12) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (63323-321-02)

Marketing

Marketing Status
Marketed Since 2009-11-17
Brand polymyxin b
Generic polymyxin b sulfate
Sample Package No

Linked Drug Pages (1)

POLYMYXIN B ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRATHECAL", "INTRAVENOUS", "OPHTHALMIC"], "spl_id": "b473292e-e7ce-4ce2-aec7-91604b82bb11", "openfda": {"upc": ["0363323321024"], "unii": ["19371312D4"], "rxcui": ["204509"], "spl_set_id": ["704a41f5-b109-4c16-8d3e-1495c9917952"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (63323-321-12)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (63323-321-02)", "package_ndc": "63323-321-12", "marketing_start_date": "20091117"}], "brand_name": "POLYMYXIN B", "product_id": "63323-321_b473292e-e7ce-4ce2-aec7-91604b82bb11", "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"}