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Diclofenac Sodium Delayed Release

NDC 51655-280, Diclofenac Sodium, tablet, delayed release, from Northwind Health Company, LLC.

Product NDC
51655-280
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075185
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-280 \
  -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
51655-280-265165502802690 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-280-26)
51655-280-525165502805230 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-280-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f2b7ea75-738b-54a8-e053-2995a90a00d5

Use it

Look up 51655-280 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-280 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-280. 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.