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Duloxetine Delayed-Release

NDC 50090-6889, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from A-S Medication Solutions.

Product NDC
50090-6889
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
CAPSULE, DELAYED RELEASE PELLETS
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203088
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6889 \
  -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
50090-6889-05009068890090 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-6889-0)
50090-6889-15009068890130 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-6889-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/be33f3cb-6fd1-4377-816e-84bd49370e9e

Use it

Look up 50090-6889 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6889 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-6889. 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.