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Duloxetine Delayed-Release

NDC 68788-8362, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8362
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
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/68788-8362 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68788-8362-06878883620060 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-0)
68788-8362-36878883620330 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-3)
68788-8362-96878883620990 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2c233b3f-83de-40c4-9f1d-81f901f89459

Use it

Look up 68788-8362 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8362 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8362. 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.