Package 69292-552-50

Brand: diclofenac potassium

Generic: diclofenac potassium, film coated
NDC Package

Package Facts

Identity

Package NDC 69292-552-50
Digits Only 6929255250
Product NDC 69292-552
Product ID 69292-552_796bf62e-3eee-423f-9770-a2d436fe5064
Description

500 TABLET in 1 BOTTLE (69292-552-50)

Marketing

Marketing Status
Marketed Since 2024-03-12
Brand diclofenac potassium
Generic diclofenac potassium, film coated
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": "796bf62e-3eee-423f-9770-a2d436fe5064", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["c4ce1497-9cb1-4632-b1a2-4f61043c018d"], "manufacturer_name": ["Amici Pharma, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69292-552-01)", "package_ndc": "69292-552-01", "marketing_start_date": "20240312"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69292-552-50)", "package_ndc": "69292-552-50", "marketing_start_date": "20240312"}], "brand_name": "DICLOFENAC POTASSIUM", "product_id": "69292-552_796bf62e-3eee-423f-9770-a2d436fe5064", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69292-552", "generic_name": "diclofenac potassium, film coated", "labeler_name": "Amici Pharma, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICLOFENAC POTASSIUM", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA215787", "marketing_category": "ANDA", "marketing_start_date": "20240312", "listing_expiration_date": "20261231"}