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Diclofenac Sodium

NDC 85509-1201, Diclofenac Sodium, tablet, delayed release, from PHOENIX RX LLC.

Product NDC
85509-1201
Status
Listed
Labeler
PHOENIX RX LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077863
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1201 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM75 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
85509-1201-38550912010330 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-3)
85509-1201-68550912010660 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (85509-1201-6)
85509-1201-98550912010990 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/47ce6fab-be1d-0076-e063-6294a90add63

Use it

Look up 85509-1201 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1201 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85509-1201. 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.