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Glipizide

NDC 70518-4128, Glipizide, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-4128
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206928
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4128 \
  -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
70518-4128-17051841280190 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4128-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/667dd68a-d3e7-4b50-bd0a-d17783a090d5

Use it

Look up 70518-4128 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4128 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4128. 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.