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Glipizide

NDC 71205-041, Glipizide, tablet, from Proficient Rx LP.

Product NDC
71205-041
Status
Listed
Labeler
Proficient Rx LP
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/71205-041 \
  -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
71205-041-307120500413030 TABLET in 1 BOTTLE (71205-041-30)
71205-041-607120500416060 TABLET in 1 BOTTLE (71205-041-60)
71205-041-7871205004178180 TABLET in 1 BOTTLE (71205-041-78)
71205-041-907120500419090 TABLET in 1 BOTTLE (71205-041-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f280acc1-d912-4f2e-b131-440e708c7b1f

Use it

Look up 71205-041 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-041. 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.