Package 69315-506-09
Brand: diclofenac potassium
Generic: diclofenac potassiumPackage Facts
Identity
Package NDC
69315-506-09
Digits Only
6931550609
Product NDC
69315-506
Description
9 PACKET in 1 CARTON (69315-506-09) / 1 POWDER, FOR SOLUTION in 1 PACKET
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": "9c24af27-0a21-4fb7-a8fb-55c92373b852", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["859063"], "spl_set_id": ["9dd418b2-4b0e-498c-b453-f580c69ddc6d"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 PACKET in 1 CARTON (69315-506-09) / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "69315-506-09", "marketing_start_date": "20221220"}], "brand_name": "DICLOFENAC POTASSIUM", "product_id": "69315-506_9c24af27-0a21-4fb7-a8fb-55c92373b852", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69315-506", "generic_name": "DICLOFENAC POTASSIUM", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICLOFENAC POTASSIUM", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "NDA022165", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20221220", "listing_expiration_date": "20261231"}