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Glipizide and Metformin Hydrochloride

NDC 70518-0373, Glipizide and Metformin Hydrochloride, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-0373
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077270
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0373 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIPIZIDE5 mg/1
  • METFORMIN HYDROCHLORIDE500 mg/1

Pharmacologic classes

Biguanide [EPC]; Biguanides [CS]; Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
70518-0373-07051803730090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0373-0)
70518-0373-170518037301180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0373-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3f2599c6-9e33-487e-9379-6477bb121461

Use it

Look up 70518-0373 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0373 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-0373. 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.