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Amlodipine and Olmesartan Medoxomil

NDC 42291-002, Amlodipine and Olmesartan Medoxomil, tablet, film coated, from AvKARE.

Product NDC
42291-002
Status
Listed
Labeler
AvKARE
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209010
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42291-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE5 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
42291-002-304229100023030 TABLET, FILM COATED in 1 BOTTLE (42291-002-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b30c3fe-5c84-0d42-e063-6394a90a81d8

Use it

Look up 42291-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42291-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42291-002. 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.