Package 69292-548-30
Brand: diclofenac potassium
Generic: diclofenac potassiumPackage Facts
Identity
Package NDC
69292-548-30
Digits Only
6929254830
Product NDC
69292-548
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69292-548-30)
Marketing
Marketing Status
Brand
diclofenac potassium
Generic
diclofenac potassium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf4973de-8da2-4fdf-8f48-938627e09d5a", "openfda": {"upc": ["0369292548301"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942", "857702"], "spl_set_id": ["f2908870-a517-491f-8771-4100d11b4b64"], "manufacturer_name": ["Amici Pharma Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69292-548-30)", "package_ndc": "69292-548-30", "marketing_start_date": "20240418"}], "brand_name": "Diclofenac Potassium", "product_id": "69292-548_cf4973de-8da2-4fdf-8f48-938627e09d5a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69292-548", "generic_name": "diclofenac potassium", "labeler_name": "Amici Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA076561", "marketing_category": "ANDA", "marketing_start_date": "20240418", "listing_expiration_date": "20261231"}