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FESOTERODINE FUMARATE

NDC 72603-414, FESOTERODINE FUMARATE, tablet, film coated, extended release, from NorthStar RxLLC.

Product NDC
72603-414
Status
Listed
Labeler
NorthStar RxLLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204792
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72603-414 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE8 mg/1
Package NDCNDC-11Package
72603-414-017260304140130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-414-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cb597206-1c75-4a4f-a17a-524a2010a4b9

  • NADAC price for package 72603041401

    GET /v1/drugs/nadac/72603041401

Use it

Look up 72603-414 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-414 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-414. 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.