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Duloxetine

NDC 25000-610, Duloxetine Hydrochloride, capsule, delayed release, from MARKSANS PHARMA LIMITED.

Product NDC
25000-610
Status
Listed
Labeler
MARKSANS PHARMA LIMITED
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090723
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25000-610 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE60 mg/1

Pharmacologic classes

Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Package NDCNDC-11Package
25000-610-032500006100330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-610-03)
25000-610-072500006100790 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-610-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3686cde5-f76d-4d16-aa5d-caceb8408f8c

Use it

Look up 25000-610 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25000-610 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25000-610. 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.