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Duloxetine

NDC 59651-279, Duloxetine Hydrochloride, capsule, delayed release, from Aurobindo Pharma Limited.

Product NDC
59651-279
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090778
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-279 \
  -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
59651-279-605965102796060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-60)
59651-279-785965102797810 BLISTER PACK in 1 CARTON (59651-279-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-279-10)
59651-279-99596510279991000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3adfceb3-5f89-4bcf-b874-e3cb572a98b6

Use it

Look up 59651-279 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-279 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-279. 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.