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telmisartan

NDC 72789-371, telmisartan, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-371
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205150
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-371 \
  -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
72789-371-907278903719090 TABLET in 1 BOTTLE, PLASTIC (72789-371-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56a72ddf-c2a2-45ce-91b1-1fcfbff52c10

Use it

Look up 72789-371 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-371 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-371. 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.