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Duloxetine

NDC 82009-172, Duloxetine, capsule, delayed release, from Quallent Pharmaceuticals Health LLC.

Product NDC
82009-172
Status
Listed
Labeler
Quallent Pharmaceuticals Health 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/82009-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
82009-172-308200901723030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-172-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b3b26383-9924-40f9-b4bb-43e30b70493e

  • NADAC price for package 82009017230

    GET /v1/drugs/nadac/82009017230

Use it

Look up 82009-172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82009-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82009-172. 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.