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Duloxetine Delayed-Release

NDC 51407-819, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from Golden State Medical Supply, Inc..

Product NDC
51407-819
Status
Listed
Labeler
Golden State Medical Supply, Inc.
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/51407-819 \
  -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
51407-819-10514070819101000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-819-10)
51407-819-305140708193030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-819-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/00628e5e-4c5b-2573-e063-6294a90a0e3b

Use it

Look up 51407-819 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51407-819 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51407-819. 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.