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DICLOFENAC POTASSIUM

NDC 71337-046, diclofenac potassium, film coated, tablet, from Havix Group Inc d-b-a Aavis Pharmaceuticals.

Product NDC
71337-046
Status
Listed
Labeler
Havix Group Inc d-b-a Aavis Pharmaceuticals
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215787
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71337-046 \
  -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
71337-046-0171337004601100 TABLET in 1 BOTTLE (71337-046-01)
71337-046-0571337004605500 TABLET in 1 BOTTLE (71337-046-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/30ab7b30-cc90-4b84-8caf-21058f1d37fa

Use it

Look up 71337-046 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71337-046 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71337-046. 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.