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Diclofenac Sodium

NDC 51672-1369, Diclofenac Sodium, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1369
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208098
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1369 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM20 mg/g

Pharmacologic classes

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

Package NDCNDC-11Package
51672-1369-8516721369081 BOTTLE, PUMP in 1 CARTON (51672-1369-8) / 112 g in 1 BOTTLE, PUMP

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f9a0c654-5f77-430f-b921-295eb776cbcd

  • NADAC price for package 51672136908

    GET /v1/drugs/nadac/51672136908

Use it

Look up 51672-1369 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1369 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1369. 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.