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Metformin hydrochloride

NDC 68682-018, metformin hydrochloride, tablet, film coated, extended release, from Oceanside Pharmaceuticals.

Product NDC
68682-018
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021748
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-018 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METFORMIN HYDROCHLORIDE1000 mg/1

Pharmacologic classes

Biguanide [EPC]; Biguanides [CS]

Package NDCNDC-11Package
68682-018-906868200189090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-018-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/74d32a8a-c4c2-4dbb-b376-eea3f8fa64d7

Use it

Look up 68682-018 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-018 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-018. 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.