Package 67046-1522-3

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 67046-1522-3
Digits Only 6704615223
Product NDC 67046-1522
Product ID 67046-1522_2eead003-b307-8679-e063-6394a90ab68a
Description

30 TABLET, COATED in 1 BLISTER PACK (67046-1522-3)

Marketing

Marketing Status
Marketed Since 2025-02-24
Brand diclofenac potassium
Generic diclofenac potassium
Sample Package No

Linked Drug Pages (1)

Diclofenac Potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2eead003-b307-8679-e063-6394a90ab68a", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["2eead069-f954-abb2-e063-6394a90a14ff"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BLISTER PACK (67046-1522-3)", "package_ndc": "67046-1522-3", "marketing_start_date": "20250224"}], "brand_name": "Diclofenac Potassium", "product_id": "67046-1522_2eead003-b307-8679-e063-6394a90ab68a", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "67046-1522", "generic_name": "diclofenac potassium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075229", "marketing_category": "ANDA", "marketing_start_date": "20250224", "listing_expiration_date": "20261231"}