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Ranolazine

NDC 13668-759, Ranolazine, tablet, film coated, extended release, from Torrent Pharma, Inc..

Product NDC
13668-759
Status
Listed
Labeler
Torrent Pharma, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214035
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/13668-759 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RANOLAZINE500 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
13668-759-601366807596060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (13668-759-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d2454377-2abd-4d9f-85f1-12f1adbb10e5

Use it

Look up 13668-759 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/13668-759 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 13668-759. 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.