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Duloxetine Hydrochloride

NDC 33342-161, Duloxetine Hydrochloride, capsule, delayed release, from Macleods Pharmaceuticals Limited.

Product NDC
33342-161
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204815
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-161 \
  -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
33342-161-073334201610730 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-07)
33342-161-103334201611090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-10)
33342-161-123334201611210 BLISTER PACK in 1 CARTON (33342-161-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
33342-161-44333420161441000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-44)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/177ce798-3924-416b-ba37-23dfa911a43b

Use it

Look up 33342-161 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-161 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-161. 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.