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Glipizide

NDC 71335-9742, Glipizide, tablet, extended release, from Bryant Ranch Prepack.

Product NDC
71335-9742
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206928
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-9742 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIPIZIDE5 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
71335-9742-17133597420190 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-1)
71335-9742-27133597420230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-2)
71335-9742-37133597420360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-3)
71335-9742-471335974204100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4afa67b2-7f86-4189-93a5-6a605f74540d

Use it

Look up 71335-9742 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-9742 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-9742. 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.