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Donepezil Hydrochloride

NDC 50228-139, Donepezil Hydrochloride, tablet, film coated, from ScieGen Pharmaceuticals, Inc..

Product NDC
50228-139
Status
Listed
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203907
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50228-139 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DONEPEZIL HYDROCHLORIDE5 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC]; Cholinesterase Inhibitors [MoA]

Package NDCNDC-11Package
50228-139-10502280139101000 TABLET, FILM COATED in 1 BOTTLE (50228-139-10)
50228-139-305022801393030 TABLET, FILM COATED in 1 BOTTLE (50228-139-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6e9aacf9-abb6-4dec-9a8d-4eabf934d512

Use it

Look up 50228-139 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50228-139 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50228-139. 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.