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Glipizide

NDC 71335-0618, Glipizide, tablet, from Bryant Ranch Prepack.

Product NDC
71335-0618
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075795
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0618 \
  -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
71335-0618-17133506180160 TABLET in 1 BOTTLE (71335-0618-1)
71335-0618-27133506180230 TABLET in 1 BOTTLE (71335-0618-2)
71335-0618-371335061803100 TABLET in 1 BOTTLE (71335-0618-3)
71335-0618-471335061804120 TABLET in 1 BOTTLE (71335-0618-4)
71335-0618-57133506180590 TABLET in 1 BOTTLE (71335-0618-5)
71335-0618-67133506180620 TABLET in 1 BOTTLE (71335-0618-6)
71335-0618-771335061807180 TABLET in 1 BOTTLE (71335-0618-7)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4995328f-287c-4d4a-9b5f-9d354cc530fb

Use it

Look up 71335-0618 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0618 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0618. 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.