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Galantamine

NDC 24979-722, galantamine, tablet, film coated, from Upsher-Smith Laboratories, LLC.

Product NDC
24979-722
Status
Listed
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077604
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24979-722 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GALANTAMINE HYDROBROMIDE4 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC]; Cholinesterase Inhibitors [MoA]

Package NDCNDC-11Package
24979-722-042497907220460 TABLET, FILM COATED in 1 BOTTLE (24979-722-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/10497273-d907-0514-e063-6294a90a1362

  • NADAC price for package 24979072204

    GET /v1/drugs/nadac/24979072204

Use it

Look up 24979-722 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24979-722 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24979-722. 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.