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METFORMIN HYDROCHLORIDE

NDC 69367-412, METFORMIN HYDROCHLORIDE, tablet, film coated, extended release, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-412
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203832
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-412 \
  -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
69367-412-606936704126060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69367-412-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/07b4ee2a-8435-4d38-a6b0-b919e3424153

  • NADAC price for package 69367041260

    GET /v1/drugs/nadac/69367041260

Use it

Look up 69367-412 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-412 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-412. 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.