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TOFACITINIB

NDC 70095-008, Tofacitinib, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
70095-008
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218407
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70095-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TOFACITINIB CITRATE1 mg/mL

Pharmacologic classes

Janus Kinase Inhibitor [EPC]; Janus Kinase Inhibitors [MoA]

Package NDCNDC-11Package
70095-008-02700950008021 BOTTLE in 1 CARTON (70095-008-02) / 240 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a764a133-b870-4514-bbee-24d43f8cb7fd

Use it

Look up 70095-008 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70095-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70095-008. 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.