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Duloxetine

NDC 70518-2630, Duloxetine, capsule, delayed release, from REMEDYREPACK INC..

Product NDC
70518-2630
Status
Listed
Labeler
REMEDYREPACK INC.
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/70518-2630 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE60 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-2630-27051826300290 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-2)
70518-2630-370518263003180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-3)
70518-2630-470518263004100 POUCH in 1 BOX (70518-2630-4) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-2630-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ac903bda-76af-4aba-9c8a-ebf7066e05ee

Use it

Look up 70518-2630 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2630 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2630. 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.