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Glipizide

NDC 68788-0142, Glipizide, tablet, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-0142
Status
Listed
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075795
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-0142 \
  -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
68788-0142-168788014201100 TABLET in 1 BOTTLE (68788-0142-1)
68788-0142-36878801420330 TABLET in 1 BOTTLE (68788-0142-3)
68788-0142-66878801420660 TABLET in 1 BOTTLE (68788-0142-6)
68788-0142-96878801420990 TABLET in 1 BOTTLE (68788-0142-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/097424ef-612f-4bc2-809a-e5bb8eeae244

Use it

Look up 68788-0142 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-0142 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-0142. 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.