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Glipizide

NDC 68788-4061, Glipizide, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4061
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074378
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4061 \
  -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
68788-4061-168788406101100 TABLET in 1 BOTTLE (68788-4061-1)
68788-4061-36878840610330 TABLET in 1 BOTTLE (68788-4061-3)
68788-4061-66878840610660 TABLET in 1 BOTTLE (68788-4061-6)
68788-4061-868788406108180 TABLET in 1 BOTTLE (68788-4061-8)
68788-4061-96878840610990 TABLET in 1 BOTTLE (68788-4061-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/410bf280-838d-45af-9b60-15f94ded7581

Use it

Look up 68788-4061 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4061 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4061. 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.