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Galantamine

NDC 70436-004, galantamine, tablet, film coated, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-004
Status
Listed
Labeler
Slate Run Pharmaceuticals, 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/70436-004 \
  -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
70436-004-067043600040660 TABLET, FILM COATED in 1 BOTTLE (70436-004-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56f365e5-0a23-4f69-e054-00144ff8d46c

Use it

Look up 70436-004 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-004 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-004. 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.