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Duloxetine

NDC 71335-2017, Duloxetine, capsule, delayed release, from Bryant Ranch Prepack.

Product NDC
71335-2017
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2017 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71335-2017-17133520170130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-1)
71335-2017-27133520170260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-2)
71335-2017-37133520170328 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-3)
71335-2017-4713352017046 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-4)
71335-2017-57133520170590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-5)
71335-2017-67133520170615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-6)
71335-2017-771335201707180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-7)
71335-2017-871335201708120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3fbdcc34-6166-4843-839c-33fed718ffb2

Use it

Look up 71335-2017 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2017 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2017. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.