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Ranolazine

NDC 42291-774, RANOLAZINE, tablet, film coated, extended release, from AvKARE.

Product NDC
42291-774
Status
Listed
Labeler
AvKARE
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212781
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42291-774 \
  -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
42291-774-604229107746060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-774-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b2a8dc3e-a880-5241-e053-2995a90a933a

Use it

Look up 42291-774 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42291-774 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42291-774. 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.