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Donepezil Hydrochloride

NDC 62756-194, Donepezil Hydrochloride, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-194
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204293
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-194 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DONEPEZIL HYDROCHLORIDE23 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC]; Cholinesterase Inhibitors [MoA]

Package NDCNDC-11Package
62756-194-18627560194181000 TABLET, FILM COATED in 1 BOTTLE (62756-194-18)
62756-194-816275601948190 TABLET, FILM COATED in 1 BOTTLE (62756-194-81)
62756-194-836275601948330 TABLET, FILM COATED in 1 BOTTLE (62756-194-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/79ad107b-bb20-4ed3-89f0-d7c862f3957c

Use it

Look up 62756-194 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-194 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-194. 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.