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Amlodipine and Olmesartan Medoxomil

NDC 65862-857, Amlodipine and Olmesartan Medoxomil, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-857
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206906
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-857 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE10 mg/1
  • OLMESARTAN MEDOXOMIL40 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]; Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A Inhibitors [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]

Package NDCNDC-11Package
65862-857-306586208573030 TABLET, FILM COATED in 1 BOTTLE (65862-857-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b13a8b46-104e-4b75-8f4a-928d2204eff5

  • NADAC price for package 65862085730

    GET /v1/drugs/nadac/65862085730

Use it

Look up 65862-857 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-857 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-857. 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.