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Cevimeline

NDC 63304-479, Cevimeline, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
63304-479
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020989
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-479 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEVIMELINE HYDROCHLORIDE30 mg/1

Pharmacologic classes

Cholinergic Muscarinic Agonists [MoA]; Cholinergic Receptor Agonist [EPC]

Package NDCNDC-11Package
63304-479-0163304047901100 CAPSULE in 1 BOTTLE (63304-479-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/773a19e8-4c3e-4414-99a6-aea98c9790ee

  • NADAC price for package 63304047901

    GET /v1/drugs/nadac/63304047901

Use it

Look up 63304-479 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-479 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-479. 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.