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Glipizide

NDC 80425-0437, Glipizide, tablet, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0437
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074497
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0437 \
  -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
80425-0437-18042504370130 TABLET in 1 BOTTLE (80425-0437-1)
80425-0437-28042504370260 TABLET in 1 BOTTLE (80425-0437-2)
80425-0437-38042504370390 TABLET in 1 BOTTLE (80425-0437-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/213c4e61-9bb7-9d1b-e063-6394a90a7339

Use it

Look up 80425-0437 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0437 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0437. 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.