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Duloxetine

NDC 65841-799, Duloxetine, capsule, delayed release, from Zydus Lifesciences Limited.

Product NDC
65841-799
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090739
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65841-799 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
65841-799-066584107990630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-06)
65841-799-146584107991460 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-14)
65841-799-166584107991690 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f36b414e-ace4-4f04-a80f-75bb25db430d

Use it

Look up 65841-799 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-799 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-799. 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.