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DICLOFENAC SODIUM

NDC 82868-101, DICLOFENAC SODIUM, tablet, delayed release, from Northwind Health Company, LLC.

Product NDC
82868-101
Status
Listed
Labeler
Northwind Health Company, LLC
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/82868-101 \
  -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
82868-101-308286801013030 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (82868-101-30)
82868-101-908286801019090 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (82868-101-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4dde6e36-7540-1cc3-e063-6294a90a3941

Use it

Look up 82868-101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82868-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82868-101. 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.