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Diclofenac Sodium

NDC 67046-1482, Diclofenac Sodium, tablet, delayed release, from Coupler LLC.

Product NDC
67046-1482
Status
Listed
Labeler
Coupler LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077863
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1482 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM75 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
67046-1482-36704614820330 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1482-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2ce0741a-7bc7-8aec-e063-6294a90ae9ef

Use it

Look up 67046-1482 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1482 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1482. 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.