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LACOSAMIDE

NDC 70710-1886, Lacosamide, injection, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1886
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209465
DEA schedule
CV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1886 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACOSAMIDE10 mg/mL

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
70710-1886-67071018860610 VIAL in 1 CARTON (70710-1886-6) / 20 mL in 1 VIAL (70710-1886-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/16a9afd2-35a6-44a9-b1d9-ca195c8640d7

Use it

Look up 70710-1886 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1886 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1886. 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.