polymyxin b
Generic: polymyxin b sulfate
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
polymyxin b
Generic Name
polymyxin b sulfate
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
polymyxin b sulfate 500000 [iU]/1
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9941
Product ID
0143-9941_dc529b6b-bbf4-44da-a829-f506c41d47f6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA060716
Listing Expiration
2026-12-31
Marketing Start
1998-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439941
Hyphenated Format
0143-9941
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
polymyxin b (source: ndc)
Generic Name
polymyxin b sulfate (source: ndc)
Application Number
ANDA060716 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500000 [iU]/1
Packaging
- 10 VIAL in 1 CARTON (0143-9941-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9941-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRATHECAL", "INTRAVENOUS", "OPHTHALMIC"], "spl_id": "dc529b6b-bbf4-44da-a829-f506c41d47f6", "openfda": {"unii": ["19371312D4"], "rxcui": ["204509"], "spl_set_id": ["18daf0d1-b6f5-46f4-ab2f-01a594f3959c"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9941-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9941-01)", "package_ndc": "0143-9941-10", "marketing_start_date": "19980601"}], "brand_name": "Polymyxin B", "product_id": "0143-9941_dc529b6b-bbf4-44da-a829-f506c41d47f6", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "0143-9941", "generic_name": "Polymyxin B sulfate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Polymyxin B", "active_ingredients": [{"name": "POLYMYXIN B SULFATE", "strength": "500000 [iU]/1"}], "application_number": "ANDA060716", "marketing_category": "ANDA", "marketing_start_date": "19980601", "listing_expiration_date": "20261231"}