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Diclofenac Potassium

NDC 66267-070, Diclofenac Potassium, tablet, film coated, from NuCare Pharmaceuticals, Inc..

Product NDC
66267-070
Status
Listed
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075219
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/66267-070 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC POTASSIUM50 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
66267-070-306626700703030 TABLET, FILM COATED in 1 BOTTLE (66267-070-30)
66267-070-606626700706060 TABLET, FILM COATED in 1 BOTTLE (66267-070-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3da9e463-1b2f-54c0-e054-00144ff88e88

Use it

Look up 66267-070 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66267-070 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66267-070. 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.