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Glipizide

NDC 16714-895, Glipizide, tablet, extended release, from Northstar Rx LLC..

Product NDC
16714-895
Status
Listed
Labeler
Northstar Rx LLC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203499
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-895 \
  -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
16714-895-0116714089501100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-895-01)
16714-895-0216714089502500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-895-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/915636a4-092e-4e2e-9bc0-0d387d996977

  • NADAC price for package 16714089501

    GET /v1/drugs/nadac/16714089501

  • NADAC price for package 16714089502

    GET /v1/drugs/nadac/16714089502

Use it

Look up 16714-895 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-895 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-895. 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.