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Glipizide

NDC 60687-701, Glipizide, tablet, from American Health Packaging.

Product NDC
60687-701
Status
Listed
Labeler
American Health Packaging
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/60687-701 \
  -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
60687-701-0160687070101100 BLISTER PACK in 1 CARTON (60687-701-01) / 1 TABLET in 1 BLISTER PACK (60687-701-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff6805bb-b5f0-46d3-bf1d-3333b63ff1ae

  • NADAC price for package 60687070101

    GET /v1/drugs/nadac/60687070101

Use it

Look up 60687-701 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-701 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-701. 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.