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Glipizide

NDC 72162-2103, Glipizide, tablet, from Bryant Ranch Prepack.

Product NDC
72162-2103
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/72162-2103 \
  -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
72162-2103-0721622103001000 TABLET in 1 BOTTLE (72162-2103-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/560448dd-3690-43d9-9667-925f20bb816e

Use it

Look up 72162-2103 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2103 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-2103. 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.