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Duloxetine

NDC 0228-2890, Duloxetine, capsule, delayed release pellets, from Actavis Pharma, Inc..

Product NDC
0228-2890
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
CAPSULE, DELAYED RELEASE PELLETS
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090776
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0228-2890 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0228-2890-060022828900660 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2890-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9dab9154-b86f-40dc-a4d1-18e6534dbc78

  • NADAC price for package 00228289006

    GET /v1/drugs/nadac/00228289006

Use it

Look up 0228-2890 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0228-2890 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0228-2890. 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.