Skip to content
healthcare.dev

olmesartan medoxomil

NDC 70518-4316, olmesartan medoxomil, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4316
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208130
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4316 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLMESARTAN MEDOXOMIL20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-4316-070518431600100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4316-0)
70518-4316-17051843160190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4316-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fe6e39da-fb6e-46da-9c03-c765020a7c87

Use it

Look up 70518-4316 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4316 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4316. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.