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Telmisartan

NDC 65862-868, Telmisartan, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-868
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206511
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-868 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TELMISARTAN40 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]

Package NDCNDC-11Package
65862-868-03658620868033 BLISTER PACK in 1 CARTON (65862-868-03) / 10 TABLET in 1 BLISTER PACK (65862-868-10)
65862-868-306586208683030 TABLET in 1 BOTTLE (65862-868-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fef6532d-438a-435e-a61f-216dd8551339

  • NADAC price for package 65862086803

    GET /v1/drugs/nadac/65862086803

  • NADAC price for package 65862086830

    GET /v1/drugs/nadac/65862086830

Use it

Look up 65862-868 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-868 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-868. 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.