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Duloxetine HCL DR

NDC 80425-0012, Duloxetine HCL, capsule, delayed release, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0012
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203197
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0012 \
  -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
80425-0012-18042500120130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0012-1)
80425-0012-28042500120260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0012-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/af6f8abd-19ec-69e4-e053-2a95a90ab69e

Use it

Look up 80425-0012 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0012 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0012. 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.