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Duloxetine D/R

NDC 72189-661, Duloxetine D/R, capsule, delayed release, from Direct_Rx.

Product NDC
72189-661
Status
Listed
Labeler
Direct_Rx
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208706
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-661 \
  -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
72189-661-307218906613030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-661-30)
72189-661-607218906616060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-661-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4a66fde2-4cce-b92e-e063-6294a90a63ee

Use it

Look up 72189-661 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-661 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-661. 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.