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Azathioprine

NDC 68682-231, Azathioprine, tablet, from Oceanside Pharmaceuticals.

Product NDC
68682-231
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075252
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-231 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AZATHIOPRINE75 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68682-231-0168682023101100 TABLET in 1 BOTTLE (68682-231-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d72ede2c-1a9b-4717-80a7-b76a6a499936
  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=68682-231

Use it

Look up 68682-231 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-231 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-231. 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.