Package 25021-196-10

Brand: polymyxin b

Generic: polymyxin b sulfate
NDC Package

Package Facts

Identity

Package NDC 25021-196-10
Digits Only 2502119610
Product NDC 25021-196
Description

10 VIAL in 1 CARTON (25021-196-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-10-01
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"], "spl_id": "1d99f0e9-015c-4be1-b110-bdd156846dd1", "openfda": {"unii": ["19371312D4"], "rxcui": ["204509"], "spl_set_id": ["7dc505aa-64b0-4b7f-8ee3-2945bde40a34"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-196-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "25021-196-10", "marketing_start_date": "20251001"}], "brand_name": "Polymyxin B", "product_id": "25021-196_1d99f0e9-015c-4be1-b110-bdd156846dd1", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "25021-196", "generic_name": "Polymyxin B Sulfate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Polymyxin B", "active_ingredients": [{"name": "POLYMYXIN B SULFATE", "strength": "500000 [USP'U]/1"}], "application_number": "ANDA207322", "marketing_category": "ANDA", "marketing_start_date": "20251001", "listing_expiration_date": "20261231"}