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Duloxetine Delayed-Release

NDC 71335-0165, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from Bryant Ranch Prepack.

Product NDC
71335-0165
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
CAPSULE, DELAYED RELEASE PELLETS
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203088
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0165 \
  -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
71335-0165-17133501650130 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-1)
71335-0165-27133501650260 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-2)
71335-0165-37133501650328 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-3)
71335-0165-47133501650490 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0165-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a891f20f-83ff-4960-81ef-9e74d01a452e

Use it

Look up 71335-0165 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0165 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0165. 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.