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Duloxetine

NDC 51655-237, Duloxetine, capsule, delayed release, from Northwind Health Company, LLC.

Product NDC
51655-237
Status
Listed
Labeler
Northwind Health Company, LLC
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/51655-237 \
  -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
51655-237-255165502372560 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-237-25)
51655-237-265165502372690 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-237-26)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c194a7b0-1e7e-a32b-e053-2995a90a7dbd

Use it

Look up 51655-237 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-237 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-237. 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.