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Glipizide

NDC 11788-120, Glipizide, tablet, from AiPing Pharmaceutical, Inc..

Product NDC
11788-120
Status
Listed
Labeler
AiPing Pharmaceutical, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074305
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/11788-120 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIPIZIDE2.5 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
11788-120-0111788012001100 TABLET in 1 BOTTLE (11788-120-01)
11788-120-0511788012005500 TABLET in 1 BOTTLE (11788-120-05)
11788-120-10117880120101000 TABLET in 1 BOTTLE (11788-120-10)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2110a7ca-3c1f-4db4-9211-65546b74533c

Use it

Look up 11788-120 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11788-120 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11788-120. 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.