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Fesoterodine Fumarate

NDC 62332-175, Fesoterodine Fumarate, tablet, extended release, from Alembic Pharmaceuticals Inc..

Product NDC
62332-175
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
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/62332-175 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE4 mg/1
Package NDCNDC-11Package
62332-175-1062332017510100 TABLET, EXTENDED RELEASE in 1 CARTON (62332-175-10)
62332-175-306233201753030 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-175-30)
62332-175-906233201759090 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-175-90)
62332-175-91623320175911000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-175-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/299db62d-9658-4796-b449-657fa859c5cd

  • NADAC price for package 62332017530

    GET /v1/drugs/nadac/62332017530

Use it

Look up 62332-175 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-175 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-175. 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.