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Diclofenac Sodium Delayed Release

NDC 68788-8952, Diclofenac Sodium, tablet, delayed release, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8952
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
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/68788-8952 \
  -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
68788-8952-168788895201100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-1)
68788-8952-36878889520330 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-3)
68788-8952-66878889520660 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-6)
68788-8952-868788895208120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-8)
68788-8952-96878889520990 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-8952-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e947653c-6789-4c15-82c9-4b1402f6d6ac

Use it

Look up 68788-8952 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8952 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8952. 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.