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OLMESARTAN MEDOXOMIL

NDC 70756-810, OLMESARTAN MEDOXOMIL, tablet, from Lifestar Pharma LLC.

Product NDC
70756-810
Status
Listed
Labeler
Lifestar Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207135
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70756-810 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLMESARTAN MEDOXOMIL40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70756-810-307075608103030 TABLET in 1 BOTTLE (70756-810-30)
70756-810-907075608109090 TABLET in 1 BOTTLE (70756-810-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a337a621-bf57-4aa4-8224-4356fa2cdbc4

Use it

Look up 70756-810 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70756-810 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70756-810. 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.