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Fesoterodine Fumarate

NDC 65162-370, Fesoterodine Fumarate, tablet, extended release, from Amneal Pharmaceuticals LLC.

Product NDC
65162-370
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205002
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-370 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FESOTERODINE FUMARATE8 mg/1
Package NDCNDC-11Package
65162-370-036516203700330 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-370-03)
65162-370-096516203700990 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-370-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1d3fdfcf-7406-4be0-90e9-b10c9257bf69

Use it

Look up 65162-370 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-370 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-370. 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.