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Fesoterodine Fumarate

NDC 67877-068, Fesoterodine Fumarate, tablet, extended release, from Ascend Laboratories, LLC.

Product NDC
67877-068
Status
Listed
Labeler
Ascend Laboratories, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204827
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67877-068 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE8 mg/1
Package NDCNDC-11Package
67877-068-306787700683030 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-068-30)
67877-068-906787700689090 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-068-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b1abd9cb-c480-437b-8531-e2de3e188363

  • NADAC price for package 67877006830

    GET /v1/drugs/nadac/67877006830

Use it

Look up 67877-068 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-068 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-068. 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.