diclofenac sodium

Generic: diclofenac sodium

Labeler: oceanside pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diclofenac sodium
Generic Name diclofenac sodium
Labeler oceanside pharmaceuticals
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diclofenac sodium 100 mg/1

Manufacturer
Oceanside Pharmaceuticals

Identifiers & Regulatory

Product NDC 68682-103
Product ID 68682-103_303dda9b-8a02-68c8-e063-6294a90a2d5e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075492
Listing Expiration 2026-12-31
Marketing Start 2000-02-28

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] decreased prostaglandin production [pe] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68682103
Hyphenated Format 68682-103

Supplemental Identifiers

RxCUI
855657
UPC
0368682103014
UNII
QTG126297Q

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name diclofenac sodium (source: ndc)
Generic Name diclofenac sodium (source: ndc)
Application Number ANDA075492 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-103-01)
source: ndc

Packages (1)

68682-103-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-103-01)

Ingredients (1)

diclofenac sodium (100 mg/1)

Linked Drug Pages (1)

Diclofenac Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "303dda9b-8a02-68c8-e063-6294a90a2d5e", "openfda": {"upc": ["0368682103014"], "unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["c48113e0-9f1e-4086-b18f-3204c0d2a689"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-103-01)", "package_ndc": "68682-103-01", "marketing_start_date": "20000228"}], "brand_name": "Diclofenac Sodium", "product_id": "68682-103_303dda9b-8a02-68c8-e063-6294a90a2d5e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68682-103", "generic_name": "Diclofenac Sodium", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA075492", "marketing_category": "ANDA", "marketing_start_date": "20000228", "listing_expiration_date": "20261231"}