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Duloxetine

NDC 68180-297, Duloxetine, capsule, delayed release, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-297
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
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/68180-297 \
  -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
68180-297-066818002970630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-297-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/829a4f51-c882-4b64-81f3-abfb03a52ebe

  • NADAC price for package 68180029706

    GET /v1/drugs/nadac/68180029706

Use it

Look up 68180-297 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-297 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-297. 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.