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Duloxetine

NDC 27241-164, Duloxetine, capsule, delayed release, from Ajanta Pharma USA Inc..

Product NDC
27241-164
Status
Listed
Labeler
Ajanta Pharma USA Inc.
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/27241-164 \
  -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
27241-164-302724101643030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-164-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2dde979d-b6f8-41d1-96fb-325c75ea3a74

  • NADAC price for package 27241016430

    GET /v1/drugs/nadac/27241016430

Use it

Look up 27241-164 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/27241-164 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 27241-164. 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.