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DICLOFENAC SODIUM

NDC 70518-4694, DICLOFENAC SODIUM, tablet, delayed release, from REMEDYREPACK INC..

Product NDC
70518-4694
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075281
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4694 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM50 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
70518-4694-07051846940030 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-4694-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6e6a6f98-5517-4f67-9a6a-71019ba2d773

Use it

Look up 70518-4694 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4694 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4694. 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.