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Temozolomide

NDC 70301-2009, TEMOZOLOMIDE, capsule, from OPKO Pharmaceuticals, LLC.

Product NDC
70301-2009
Status
Listed
Labeler
OPKO Pharmaceuticals, LLC
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203898
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70301-2009 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TEMOZOLOMIDE180 mg/1

Pharmacologic classes

Alkylating Activity [MoA]; Alkylating Drug [EPC]

Package NDCNDC-11Package
70301-2009-1703012009015 PACKET in 1 CARTON (70301-2009-1) / 1 CAPSULE in 1 PACKET
70301-2009-27030120090214 PACKET in 1 CARTON (70301-2009-2) / 1 CAPSULE in 1 PACKET

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f743f7e0-74cf-47e5-bf21-f2b75d2596dc

Use it

Look up 70301-2009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70301-2009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70301-2009. 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.