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Duloxetine

NDC 72789-338, Duloxetine, capsule, delayed release, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-338
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/72789-338 \
  -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
72789-338-907278903389090 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-338-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/db85a82d-84f1-41c8-964b-ac94ae4d8e7b

Use it

Look up 72789-338 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-338 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-338. 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.