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NDC 81165-100, letibotulinumtoxinA-wlbg, injection, powder, lyophilized, for solution, from Hugel, Inc..

Product NDC
81165-100
Status
Listed
Labeler
Hugel, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAMUSCULAR
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA761225
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/81165-100 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LETIBOTULINUMTOXINA100 U/1

Pharmacologic classes

Acetylcholine Release Inhibitor [EPC]; Acetylcholine Release Inhibitors [MoA]; Neuromuscular Blockade [PE]; Neuromuscular Blocker [EPC]

Package NDCNDC-11Package
81165-100-01811650100011 VIAL, SINGLE-DOSE in 1 CARTON (81165-100-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/910e5d0e-4d0b-4de8-8e2d-97879a044181

Use it

Look up 81165-100 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81165-100 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81165-100. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.