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Duloxetine

NDC 85534-0050, Duloxetine, capsule, delayed release pellets, from HAWAII REPACK, INC.

Product NDC
85534-0050
Status
Listed
Labeler
HAWAII REPACK, INC
Dosage form
CAPSULE, DELAYED RELEASE PELLETS
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090776
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85534-0050 \
  -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
85534-0050-08553400500030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (85534-0050-0)
85534-0050-18553400500160 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (85534-0050-1)
85534-0050-28553400500290 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (85534-0050-2)
85534-0050-385534005003120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (85534-0050-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b32a39d8-5f1a-4e44-bc46-b65925bde753

Use it

Look up 85534-0050 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85534-0050 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85534-0050. 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.