Package 63323-393-06

Brand: colistimethate

Generic: colistimethate sodium
NDC Package

Package Facts

Identity

Package NDC 63323-393-06
Digits Only 6332339306
Product NDC 63323-393
Description

1 VIAL in 1 BOX (63323-393-06) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2009-12-04
Brand colistimethate
Generic colistimethate sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4637a207-5042-4af6-a7a7-e63cd472b0d3", "openfda": {"unii": ["XW0E5YS77G"], "rxcui": ["1117522"], "spl_set_id": ["ab241809-0d2f-44ba-829c-26be67ee623f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (63323-393-06)  / 2 mL in 1 VIAL", "package_ndc": "63323-393-06", "marketing_start_date": "20091204"}], "brand_name": "Colistimethate", "product_id": "63323-393_4637a207-5042-4af6-a7a7-e63cd472b0d3", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "63323-393", "generic_name": "COLISTIMETHATE SODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colistimethate", "active_ingredients": [{"name": "COLISTIMETHATE SODIUM", "strength": "150 mg/2mL"}], "application_number": "ANDA065364", "marketing_category": "ANDA", "marketing_start_date": "20091204", "listing_expiration_date": "20261231"}