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POLYMYXIN B

NDC 68083-174, POLYMYXIN B SULFATE, injection, powder, lyophilized, for solution, from Gland Pharma Limited.

Product NDC
68083-174
Status
Listed
Labeler
Gland Pharma Limited
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAMUSCULAR, INTRATHECAL, INTRAVENOUS, OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207322
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68083-174 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POLYMYXIN B SULFATE500000 [USP'U]/1

Pharmacologic classes

Polymyxin-class Antibacterial [EPC]; Polymyxins [CS]

Package NDCNDC-11Package
68083-174-106808301741010 VIAL in 1 CARTON (68083-174-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (68083-174-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc74dee2-1d0b-4fab-a29b-1755fdb5da75

Use it

Look up 68083-174 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68083-174 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68083-174. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.