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Glipizide

NDC 70518-0552, Glipizide, tablet, from REMEDYREPACK INC..

Product NDC
70518-0552
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/70518-0552 \
  -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
70518-0552-07051805520030 TABLET in 1 BLISTER PACK (70518-0552-0)
70518-0552-170518055201180 TABLET in 1 BOTTLE, PLASTIC (70518-0552-1)
70518-0552-270518055202100 TABLET in 1 BOTTLE, PLASTIC (70518-0552-2)
70518-0552-37051805520390 TABLET in 1 BOTTLE, PLASTIC (70518-0552-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/212897cb-7de7-4711-aaf4-44234f950e9f

Use it

Look up 70518-0552 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0552 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-0552. 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.