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Glipizide

NDC 70518-0579, Glipizide, tablet, from REMEDYREPACK INC..

Product NDC
70518-0579
Status
Listed
Labeler
REMEDYREPACK 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/70518-0579 \
  -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
70518-0579-070518057900180 TABLET in 1 BOTTLE, PLASTIC (70518-0579-0)
70518-0579-17051805790130 TABLET in 1 BLISTER PACK (70518-0579-1)
70518-0579-27051805790290 TABLET in 1 BOTTLE, PLASTIC (70518-0579-2)
70518-0579-370518057903100 TABLET in 1 BOTTLE, PLASTIC (70518-0579-3)
70518-0579-77051805790730 TABLET in 1 BLISTER PACK (70518-0579-7)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/376ce3cf-4e1b-4b5f-b3e7-cc9fc4a5aeb4

Use it

Look up 70518-0579 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0579 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-0579. 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.