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Duloxetine

NDC 71205-005, Duloxetine, capsule, delayed release, from Proficient Rx LP.

Product NDC
71205-005
Status
Listed
Labeler
Proficient Rx LP
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208706
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-005 \
  -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
71205-005-307120500053030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-30)
71205-005-607120500056060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-60)
71205-005-907120500059090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5410084d-a7db-4da1-a45d-24b91ef50404

Use it

Look up 71205-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-005. 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.