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DICLOFENAC POTASSIUM

NDC 60290-061, Diclofenac potassium, powder, for solution, from Umedica Laboratories USA Inc..

Product NDC
60290-061
Status
Listed
Labeler
Umedica Laboratories USA Inc.
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217010
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60290-061 \
  -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
60290-061-01602900061011 POWDER, FOR SOLUTION in 1 PACKET (60290-061-01)
60290-061-02602900061029 POWDER, FOR SOLUTION in 1 CARTON (60290-061-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/33930285-dd97-415c-9e2a-491bd7b12af9

Use it

Look up 60290-061 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60290-061 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60290-061. 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.