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DULOXETINE HYDROCHLORIDE

NDC 50771-203, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from Yaopharma Co., Ltd..

Product NDC
50771-203
Status
Listed
Labeler
Yaopharma Co., Ltd.
Dosage form
CAPSULE, DELAYED RELEASE PELLETS
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207219
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50771-203 \
  -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
50771-203-015077102030130 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-01)
50771-203-0250771020302500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/90224073-178d-7ec5-e053-2995a90a20fc

Use it

Look up 50771-203 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50771-203 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50771-203. 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.