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Metformin Hydrochloride

NDC 71709-110, Metformin Hydrochloride, tablet, film coated, from Metcure Pharmaceuticals, Inc..

Product NDC
71709-110
Status
Listed
Labeler
Metcure Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090564
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71709-110 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METFORMIN HYDROCHLORIDE500 mg/1

Pharmacologic classes

Biguanide [EPC]; Biguanides [CS]

Package NDCNDC-11Package
71709-110-0671709011006500 TABLET, FILM COATED in 1 BOTTLE (71709-110-06)
71709-110-07717090110071000 TABLET, FILM COATED in 1 BOTTLE (71709-110-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5df6adc9-79fd-66ef-e053-2991aa0a75ce

Use it

Look up 71709-110 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71709-110 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71709-110. 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.