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Fesoterodine Fumarate

NDC 46708-176, Fesoterodine Fumarate, tablet, extended release, from Alembic Pharmaceuticals Limited.

Product NDC
46708-176
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204973
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-176 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE8 mg/1
Package NDCNDC-11Package
46708-176-1046708017610100 TABLET, EXTENDED RELEASE in 1 CARTON (46708-176-10)
46708-176-304670801763030 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-176-30)
46708-176-904670801769090 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-176-90)
46708-176-91467080176911000 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-176-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/571147f2-e182-44b5-9d0b-ecfc3265cc2d

Use it

Look up 46708-176 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-176 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-176. 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.