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fesoterodine fumarate

NDC 68382-479, fesoterodine fumarate, tablet, film coated, extended release, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-479
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204946
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-479 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE4 mg/1
Package NDCNDC-11Package
68382-479-066838204790630 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-479-06)
68382-479-166838204791690 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-479-16)
68382-479-776838204797710 BLISTER PACK in 1 CARTON (68382-479-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-479-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8c68e918-b47b-466d-80bc-4f521aa74607

  • NADAC price for package 68382047906

    GET /v1/drugs/nadac/68382047906

Use it

Look up 68382-479 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-479 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-479. 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.