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Glipizide

NDC 71335-2540, Glipizide, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2540
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214874
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2540 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIPIZIDE10 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
71335-2540-17133525400160 TABLET in 1 BOTTLE (71335-2540-1)
71335-2540-27133525400230 TABLET in 1 BOTTLE (71335-2540-2)
71335-2540-371335254003100 TABLET in 1 BOTTLE (71335-2540-3)
71335-2540-471335254004120 TABLET in 1 BOTTLE (71335-2540-4)
71335-2540-57133525400590 TABLET in 1 BOTTLE (71335-2540-5)
71335-2540-67133525400620 TABLET in 1 BOTTLE (71335-2540-6)
71335-2540-771335254007180 TABLET in 1 BOTTLE (71335-2540-7)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5ca7e38b-84cb-4043-b97e-e2f5cd82b442

Use it

Look up 71335-2540 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2540 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2540. 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.