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Duloxetine

NDC 52427-821, Duloxetine, capsule, delayed release, from Almatica Pharma LLC.

Product NDC
52427-821
Status
Listed
Labeler
Almatica Pharma LLC
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA219131
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52427-821 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE80 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
52427-821-305242708213030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (52427-821-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bb2ca3bf-983c-1e4a-a91d-dc7dee66d741

Use it

Look up 52427-821 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52427-821 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52427-821. 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.