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Toviaz

NDC 0069-0242, fesoterodine fumarate, tablet, film coated, extended release, from Pfizer Laboratories Div Pfizer Inc.

Product NDC
0069-0242
Status
Listed
Labeler
Pfizer Laboratories Div Pfizer Inc
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA022030
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0069-0242 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE4 mg/1
Package NDCNDC-11Package
0069-0242-300006902423030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0242-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5be745f0-8ae7-4c3c-9962-37d6263326f1

  • NADAC price for package 00069024230

    GET /v1/drugs/nadac/00069024230

Use it

Look up 0069-0242 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0069-0242 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0069-0242. 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.