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Tofacitinib

NDC 33342-542, Tofacitinib, tablet, film coated, from Macleods Pharmaceuticals Limited.

Product NDC
33342-542
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219530
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-542 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TOFACITINIB CITRATE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
33342-542-093334205420960 TABLET, FILM COATED in 1 BOTTLE (33342-542-09)
33342-542-43333420542439 BLISTER PACK in 1 CARTON (33342-542-43) / 10 TABLET, FILM COATED in 1 BLISTER PACK (33342-542-66)
33342-542-5433342054254120 TABLET, FILM COATED in 1 BOTTLE (33342-542-54)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9b654f0d-7705-4880-9e9d-ad3a51e56b56

Use it

Look up 33342-542 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-542 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-542. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.