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Duloxetine Delayed-Release

NDC 72162-1600, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from Bryant Ranch Prepack.

Product NDC
72162-1600
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/72162-1600 \
  -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
72162-1600-37216216000330 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1600-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f66f63c8-51db-4183-a452-78205cf3a263

Use it

Look up 72162-1600 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1600 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1600. 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.