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Ranolazine

NDC 31722-669, Ranolazine, tablet, film coated, extended release, from Camber Pharmaceuticals, Inc..

Product NDC
31722-669
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212788
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-669 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RANOLAZINE1000 mg/1

Pharmacologic classes

Anti-anginal [EPC]; Cytochrome P450 2D6 Inhibitors [MoA]; Cytochrome P450 3A Inhibitors [MoA]; Organic Cation Transporter 2 Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]

Package NDCNDC-11Package
31722-669-603172206696060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-669-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/82948cdb-73af-4f3f-bd03-628ed0fdbfba

  • NADAC price for package 31722066960

    GET /v1/drugs/nadac/31722066960

Use it

Look up 31722-669 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-669 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-669. 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.