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Fesoterodine Fumarate

NDC 46708-175, Fesoterodine Fumarate, tablet, extended release, from Alembic Pharmaceuticals Limited.

Product NDC
46708-175
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/46708-175 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE4 mg/1
Package NDCNDC-11Package
46708-175-1046708017510100 TABLET, EXTENDED RELEASE in 1 CARTON (46708-175-10)
46708-175-304670801753030 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-175-30)
46708-175-904670801759090 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-175-90)
46708-175-91467080175911000 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-175-91)

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 46708-175 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-175 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-175. 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.