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Duloxetine

NDC 71335-2537, Duloxetine, capsule, delayed release, from Bryant Ranch Prepack.

Product NDC
71335-2537
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2537 \
  -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
71335-2537-17133525370130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-1)
71335-2537-27133525370260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-2)
71335-2537-37133525370328 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-3)
71335-2537-4713352537046 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-4)
71335-2537-57133525370590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-5)
71335-2537-67133525370615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-6)
71335-2537-771335253707180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-7)
71335-2537-871335253708120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/39e293d5-c575-49db-8389-7ac2269c49bb

Use it

Look up 71335-2537 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2537 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2537. 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.