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PLERIXAFOR

NDC 70710-1208, plerixafor, injection, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1208
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208980
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1208 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PLERIXAFOR24 mg/1.2mL

Pharmacologic classes

Hematopoietic Stem Cell Mobilizer [EPC]; Increased Hematopoietic Stem Cell Mobilization [PE]

Package NDCNDC-11Package
70710-1208-1707101208011 VIAL, SINGLE-USE in 1 CARTON (70710-1208-1) / 1.2 mL in 1 VIAL, SINGLE-USE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a0a058f9-1618-4853-9b8a-e9768ee86b39

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70710-1208

Use it

Look up 70710-1208 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1208 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1208. 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.