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Tranylcypromine Sulfate

NDC 0591-5590, tranylcypromine sulfate, tablet, film coated, from Actavis Pharma, Inc..

Product NDC
0591-5590
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA012342
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0591-5590 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRANYLCYPROMINE SULFATE10 mg/1

Pharmacologic classes

Monoamine Oxidase Inhibitor [EPC]; Monoamine Oxidase Inhibitors [MoA]

Package NDCNDC-11Package
0591-5590-0100591559001100 TABLET, FILM COATED in 1 BOTTLE (0591-5590-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6a0b609b-0625-4c26-91a1-59ee3ece3ddf

  • NADAC price for package 00591559001

    GET /v1/drugs/nadac/00591559001

Use it

Look up 0591-5590 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0591-5590 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0591-5590. 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.