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Telmisartan

NDC 65162-291, Telmisartan, tablet, from Amneal Pharmaceuticals LLC.

Product NDC
65162-291
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204415
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-291 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TELMISARTAN20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
65162-291-036516202910330 TABLET in 1 BOTTLE (65162-291-03)
65162-291-096516202910990 TABLET in 1 BOTTLE (65162-291-09)
65162-291-5065162029150500 TABLET in 1 BOTTLE (65162-291-50)
65162-291-63651620291633 BLISTER PACK in 1 CARTON (65162-291-63) / 10 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/20a60231-64f0-4751-aa81-6c0e64334179

Use it

Look up 65162-291 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-291 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-291. 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.