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NDC 0713-0871, amlodipine besylate and olmesartan medoxomil, tablet, film coated, from Cosette Pharmaceuticals, Inc..

Product NDC
0713-0871
Status
Listed
Labeler
Cosette Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA022100
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0713-0871 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE10 mg/1
  • OLMESARTAN MEDOXOMIL20 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
0713-0871-300071308713030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0871-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c5535406-b63b-49aa-88b9-169aaf0ed08e

Use it

Look up 0713-0871 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0713-0871 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0713-0871. 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.