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fesoterodine fumarate

NDC 70771-1169, fesoterodine fumarate, tablet, film coated, extended release, from Zydus Lifesciences Limited.

Product NDC
70771-1169
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1169 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE8 mg/1
Package NDCNDC-11Package
70771-1169-37077111690330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-3)
70771-1169-47077111690410 BLISTER PACK in 1 CARTON (70771-1169-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1169-2)
70771-1169-97077111690990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/26e8cc63-1e1d-4a77-8f53-4c38bcf0d443

Use it

Look up 70771-1169 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1169 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1169. 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.