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DULOXETINE HYDROCHLORIDE

NDC 46708-279, Duloxetine, capsule, delayed release, from Alembic Pharmaceuticals Limited.

Product NDC
46708-279
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202949
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-279 \
  -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
46708-279-304670802793030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-30)
46708-279-904670802799090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-90)
46708-279-91467080279911000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/05a744a5-64ef-42d7-a19c-568be5a272d4

Use it

Look up 46708-279 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-279 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-279. 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.