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Ranolazine

NDC 63304-018, Ranolazine, tablet, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
63304-018
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211707
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-018 \
  -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
63304-018-0563304001805500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-05)
63304-018-2863304001828180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-28)
63304-018-606330400186060 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-018-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c5848232-b7fd-4fe5-a543-16d6c4b5c0b1

Use it

Look up 63304-018 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-018 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-018. 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.