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Diclofenac Sodium

NDC 71610-068, Diclofenac Sodium, tablet, delayed release, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-068
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074514
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-068 \
  -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
71610-068-8071610006880180 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-068-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e4af374a-1281-46af-a0a9-48820db6c947

Use it

Look up 71610-068 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-068 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-068. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.