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Duloxetine Delayed-Release

NDC 51991-750, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from Breckenridge Pharmaceutical, Inc..

Product NDC
51991-750
Status
Listed
Labeler
Breckenridge Pharmaceutical, 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/51991-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51991-750-0551991075005500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-05)
51991-750-10519910750101000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-10)
51991-750-335199107503330 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-33)
51991-750-905199107509090 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/caef6f50-1571-4ec7-8f8c-42b924d323ee

  • NADAC price for package 51991075033

    GET /v1/drugs/nadac/51991075033

  • NADAC price for package 51991075090

    GET /v1/drugs/nadac/51991075090

Use it

Look up 51991-750 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51991-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51991-750. 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.