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Telmisartan

NDC 70756-312, Telmisartan, tablet, from Lifestar Pharma LLC.

Product NDC
70756-312
Status
Listed
Labeler
Lifestar Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218157
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70756-312 \
  -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
70756-312-307075603123030 TABLET in 1 BOTTLE (70756-312-30)
70756-312-997075603129910 BLISTER PACK in 1 CARTON (70756-312-99) / 10 TABLET in 1 BLISTER PACK (70756-312-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3ff464e6-7a36-4544-a06f-7848414f77fc

  • NADAC price for package 70756031230

    GET /v1/drugs/nadac/70756031230

Use it

Look up 70756-312 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70756-312 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70756-312. 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.