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Duloxetine

NDC 67046-1598, Duloxetine, capsule, delayed release, from Coupler LLC.

Product NDC
67046-1598
Status
Listed
Labeler
Coupler LLC
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090694
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1598 \
  -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
67046-1598-36704615980330 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (67046-1598-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 67046-1598 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1598 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1598. 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.