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Telmisartan

NDC 46708-608, Telmisartan, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-608
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202130
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-608 \
  -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
46708-608-304670806083030 TABLET in 1 BOTTLE (46708-608-30)
46708-608-91467080608911000 TABLET in 1 BOTTLE (46708-608-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4be6575f-ea8d-4cd8-a49d-3d1c93f2621a

Use it

Look up 46708-608 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-608 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-608. 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.