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CEVIMELINE HYDROCHLORIDE

NDC 72789-457, CEVIMELINE HYDROCHLORIDE, capsule, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-457
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/72789-457 \
  -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
72789-457-0172789045701100 CAPSULE in 1 BOTTLE, PLASTIC (72789-457-01)
72789-457-307278904573030 CAPSULE in 1 BOTTLE, PLASTIC (72789-457-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2b429ea7-1c7c-47a4-803c-2546736f5c36

Use it

Look up 72789-457 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-457 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-457. 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.