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Glipizide

NDC 68788-4020, Glipizide, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4020
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214874
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4020 \
  -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
68788-4020-168788402001100 TABLET in 1 BOTTLE (68788-4020-1)
68788-4020-36878840200330 TABLET in 1 BOTTLE (68788-4020-3)
68788-4020-66878840200660 TABLET in 1 BOTTLE (68788-4020-6)
68788-4020-868788402008180 TABLET in 1 BOTTLE (68788-4020-8)
68788-4020-96878840200990 TABLET in 1 BOTTLE (68788-4020-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4d490a3a-abdc-4ff4-83fb-f302f51e3023

Use it

Look up 68788-4020 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4020 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4020. 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.