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DICLOFENAC SODIUM

NDC 68071-5319, DICLOFENAC SODIUM, tablet, delayed release, from NuCare Pharmaceuticals, Inc..

Product NDC
68071-5319
Status
Listed
Labeler
NuCare Pharmaceuticals, 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/68071-5319 \
  -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
68071-5319-16807153190121 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-5319-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5a852412-69af-6502-e063-6294a90a0748

Use it

Look up 68071-5319 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5319 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-5319. 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.