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DICLOFENAC SODIUM

NDC 68001-621, Diclofenac Sodium Topical Gel, 1%, gel, from BluePoint Laboratories.

Product NDC
68001-621
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA210986
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-621 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM10 mg/g

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
68001-621-45680010621451 TUBE in 1 CARTON (68001-621-45) / 100 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 68001062145

    GET /v1/drugs/nadac/68001062145

Use it

Look up 68001-621 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-621 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-621. 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.