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CEVIMELINE HYDROCHLORIDE

NDC 71335-2326, CEVIMELINE HYDROCHLORIDE, capsule, from Bryant Ranch Prepack.

Product NDC
71335-2326
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216682
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2326 \
  -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
71335-2326-17133523260130 CAPSULE in 1 BOTTLE, PLASTIC (71335-2326-1)
71335-2326-27133523260260 CAPSULE in 1 BOTTLE, PLASTIC (71335-2326-2)
71335-2326-37133523260390 CAPSULE in 1 BOTTLE, PLASTIC (71335-2326-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/75ae16d6-8822-4581-b747-ae894a45cdea

Use it

Look up 71335-2326 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2326 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2326. 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.