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Galantamine

NDC 65862-459, Galantamine, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-459
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090957
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-459 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GALANTAMINE HYDROBROMIDE8 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC]; Cholinesterase Inhibitors [MoA]

Package NDCNDC-11Package
65862-459-606586204596060 TABLET, FILM COATED in 1 BOTTLE (65862-459-60)
65862-459-71658620459717000 TABLET, FILM COATED in 1 BOTTLE (65862-459-71)
65862-459-99658620459991000 TABLET, FILM COATED in 1 BOTTLE (65862-459-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4e05d1da-0eb8-4fe0-8259-f1ebb170e0dc

  • NADAC price for package 65862045960

    GET /v1/drugs/nadac/65862045960

Use it

Look up 65862-459 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-459 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-459. 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.