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Glumetza

NDC 68012-004, metformin hydrochloride, tablet, film coated, extended release, from Santarus, Inc..

Product NDC
68012-004
Status
Listed
Labeler
Santarus, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021748
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68012-004 \
  -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
68012-004-5068012000450100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68012-004-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fb832474-88d9-4e29-95cd-fbc446944cc4

Use it

Look up 68012-004 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68012-004 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68012-004. 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.