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Duloxetine

NDC 71610-402, Duloxetine Hydrochloride, capsule, delayed release, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-402
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090778
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-402 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71610-402-607161004026090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-402-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b102b8e6-d58f-419c-bb35-720bafa13294

Use it

Look up 71610-402 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-402 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-402. 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.