diclofenac sodium

Generic: diclofenac sodium

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

diclofenac sodium 100 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2223
Product ID 68071-2223_1d7609b9-edfe-178d-e063-6294a90a3626
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 680712223
Hyphenated Format 68071-2223

Supplemental Identifiers

RxCUI
855657
UPC
0368071222371
UNII
QTG126297Q

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
  • 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-2223-7)
source: ndc

Packages (1)

68071-2223-7 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-2223-7)

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": "1d7609b9-edfe-178d-e063-6294a90a3626", "openfda": {"upc": ["0368071222371"], "unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["abacf60f-0410-e6da-e053-2995a90a413c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-2223-7)", "package_ndc": "68071-2223-7", "marketing_start_date": "20200730"}], "brand_name": "Diclofenac Sodium", "product_id": "68071-2223_1d7609b9-edfe-178d-e063-6294a90a3626", "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": "68071-2223", "generic_name": "Diclofenac Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}