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Duloxetine

NDC 76420-236, Duloxetine, capsule, delayed release pellets, from Asclemed USA, Inc..

Product NDC
76420-236
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
CAPSULE, DELAYED RELEASE PELLETS
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090776
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-236 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
76420-236-307642002363030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-30)
76420-236-607642002366060 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-60)
76420-236-907642002369090 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7c755ca3-0855-4b54-80a8-01b85f8e644a

Use it

Look up 76420-236 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-236 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-236. 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.