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Glimepiride

NDC 70518-4485, Glimepiride, tablet, from REMEDYREPACK INC..

Product NDC
70518-4485
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202112
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4485 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIMEPIRIDE4 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
70518-4485-070518448500100 TABLET in 1 BOTTLE, PLASTIC (70518-4485-0)
70518-4485-17051844850190 TABLET in 1 BOTTLE, PLASTIC (70518-4485-1)
70518-4485-27051844850230 TABLET in 1 BLISTER PACK (70518-4485-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c994796e-dd3d-4f40-a8f2-d317f55e34d5

Use it

Look up 70518-4485 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4485 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4485. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.