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Glipizide

NDC 16714-896, Glipizide, tablet, extended release, from Northstar Rx LLC..

Product NDC
16714-896
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/16714-896 \
  -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
16714-896-0116714089601100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-896-01)
16714-896-0216714089602500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-896-02)

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 16714089601

    GET /v1/drugs/nadac/16714089601

  • NADAC price for package 16714089602

    GET /v1/drugs/nadac/16714089602

Use it

Look up 16714-896 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-896 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-896. 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.