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Pomalidomide

NDC 70095-060, Pomalidomide, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
70095-060
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210232
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70095-060 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POMALIDOMIDE4 mg/1

Pharmacologic classes

Thalidomide Analog [EPC]

Package NDCNDC-11Package
70095-060-017009500600121 CAPSULE in 1 BOTTLE (70095-060-01)
70095-060-0270095006002100 CAPSULE in 1 BOTTLE (70095-060-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3c222961-5398-4185-b2d0-defe90230094

Use it

Look up 70095-060 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70095-060 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70095-060. 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.