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METFORMIN HYDROCHLORIDE

NDC 62756-142, METFORMIN HYDROCHLORIDE, tablet, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-142
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077336
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-142 \
  -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
62756-142-0162756014201100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01)
62756-142-0262756014202500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 62756-142 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-142 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-142. 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.