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Diclofenac Sodium

NDC 68001-279, Diclofenac Sodium, tablet, delayed release, from BluePoint Laboratories.

Product NDC
68001-279
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090066
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-279 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM25 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
68001-279-0068001027900100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-279-00)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/feb1541a-de83-47dd-be03-c43376527318

  • NADAC price for package 68001027900

    GET /v1/drugs/nadac/68001027900

Use it

Look up 68001-279 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-279 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-279. 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.