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Glipizide

NDC 70518-2308, Glipizide, tablet, film coated, extended release, from REMEDYREPACK INC..

Product NDC
70518-2308
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204720
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2308 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIPIZIDE2.5 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
70518-2308-07051823080030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2308-0)
70518-2308-17051823080190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2308-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bde478e6-e290-47e0-9241-ce88d927633e

Use it

Look up 70518-2308 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2308 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2308. 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.