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Azathioprine

NDC 67877-492, Azathioprine, tablet, from Ascend Laboratories, LLC.

Product NDC
67877-492
Status
Listed
Labeler
Ascend Laboratories, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208687
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67877-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZATHIOPRINE25 mg/1

Pharmacologic classes

Nucleic Acid Synthesis Inhibitors [MoA]; Nucleosides [CS]; Purine Antimetabolite [EPC]; Purines [CS]

Package NDCNDC-11Package
67877-492-0167877049201100 TABLET in 1 BOTTLE (67877-492-01)
67877-492-0567877049205500 TABLET in 1 BOTTLE (67877-492-05)
67877-492-10678770492101000 TABLET in 1 BOTTLE (67877-492-10)
67877-492-14678770492141 BLISTER PACK in 1 CARTON (67877-492-14) / 14 TABLET in 1 BLISTER PACK
67877-492-386787704923810 BLISTER PACK in 1 CARTON (67877-492-38) / 10 TABLET in 1 BLISTER PACK (67877-492-33)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bc6dc4bd-2121-4613-9d90-4a504010c98a

Use it

Look up 67877-492 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-492. 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.