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Glipizide

NDC 68071-4085, Glipizide, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-4085
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074223
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-4085 \
  -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
68071-4085-36807140850330 TABLET in 1 BOTTLE (68071-4085-3)
68071-4085-66807140850660 TABLET in 1 BOTTLE (68071-4085-6)
68071-4085-868071408508180 TABLET in 1 BOTTLE (68071-4085-8)
68071-4085-96807140850990 TABLET in 1 BOTTLE (68071-4085-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/589dc76d-c347-0589-e053-2991aa0a2520

Use it

Look up 68071-4085 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-4085 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-4085. 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.