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Duloxetine

NDC 47335-382, Duloxetine, capsule, delayed release, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-382
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090745
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-382 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
47335-382-0847335038208100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-08)
47335-382-18473350382181000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-18)
47335-382-6147335038261100 BLISTER PACK in 1 CARTON (47335-382-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
47335-382-814733503828190 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-81)
47335-382-834733503828330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-83)
47335-382-8847335038288100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f16beb64-5878-486a-82ee-8e83e728f26c

Use it

Look up 47335-382 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-382 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-382. 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.