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Duloxetine Delayed-Release

NDC 68071-2711, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2711
Status
Listed
Labeler
NuCare 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/68071-2711 \
  -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
68071-2711-96807127110990 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-2711-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/df61b895-c358-827b-e053-2995a90a9b60

Use it

Look up 68071-2711 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2711 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2711. 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.