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Diclofenac Sodium

NDC 68682-103, Diclofenac Sodium, tablet, film coated, extended release, from Oceanside Pharmaceuticals.

Product NDC
68682-103
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075492
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICLOFENAC SODIUM100 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
68682-103-0168682010301100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-103-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c48113e0-9f1e-4086-b18f-3204c0d2a689

Use it

Look up 68682-103 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-103 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-103. 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.