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Duloxetine

NDC 70518-1244, Duloxetine, capsule, delayed release, from REMEDYREPACK INC..

Product NDC
70518-1244
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090694
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1244 \
  -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
70518-1244-07051812440030 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-0)
70518-1244-17051812440160 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-1)
70518-1244-37051812440330 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-3)
70518-1244-47051812440450 POUCH in 1 BOX (70518-1244-4) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-1244-5)
70518-1244-67051812440650 POUCH in 1 BOX (70518-1244-6) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-1244-7)
70518-1244-87051812440890 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-8)
70518-1244-97051812440930 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/461d769c-b787-4bc7-b4a6-7a5f33ae9d45

Use it

Look up 70518-1244 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1244 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1244. 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.