polymyxin b

Generic: polymyxin b sulfate

Labeler: fosun pharma usa inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name polymyxin b
Generic Name polymyxin b sulfate
Labeler fosun pharma usa inc
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAMUSCULAR INTRATHECAL INTRAVENOUS OPHTHALMIC
Active Ingredients

polymyxin b sulfate 500000 [USP'U]/1

Manufacturer
FOSUN PHARMA USA INC

Identifiers & Regulatory

Product NDC 72266-249
Product ID 72266-249_3648864b-bfdb-b481-e063-6294a90a77b2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207322
Listing Expiration 2026-12-31
Marketing Start 2023-08-31

Pharmacologic Class

Classes
polymyxin-class antibacterial [epc] polymyxins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72266249
Hyphenated Format 72266-249

Supplemental Identifiers

RxCUI
204509
UPC
0372266249104
UNII
19371312D4

Packaging Origin

Original Packager
true

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 ANDA207322 (source: ndc)
Routes
INTRAMUSCULAR INTRATHECAL INTRAVENOUS OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 500000 [USP'U]/1
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (72266-249-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72266-249-01)
source: ndc

Packages (1)

72266-249-10 10 VIAL in 1 CARTON (72266-249-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72266-249-01)

Ingredients (1)

polymyxin b sulfate (500000 [USP'U]/1)

Linked Drug Pages (1)

POLYMYXIN B ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRATHECAL", "INTRAVENOUS", "OPHTHALMIC"], "spl_id": "3648864b-bfdb-b481-e063-6294a90a77b2", "openfda": {"upc": ["0372266249104"], "unii": ["19371312D4"], "rxcui": ["204509"], "spl_set_id": ["fd664927-db58-a1af-e053-6294a90a9048"], "manufacturer_name": ["FOSUN PHARMA USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72266-249-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72266-249-01)", "package_ndc": "72266-249-10", "marketing_start_date": "20230831"}], "brand_name": "POLYMYXIN B", "product_id": "72266-249_3648864b-bfdb-b481-e063-6294a90a77b2", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "72266-249", "generic_name": "POLYMYXIN B SULFATE", "labeler_name": "FOSUN PHARMA USA INC", "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": "20230831", "listing_expiration_date": "20261231"}