Package 49884-905-64
Brand: diclofenac potassium
Generic: diclofenac potassiumPackage Facts
Identity
Package NDC
49884-905-64
Digits Only
4988490564
Product NDC
49884-905
Description
9 POWDER, FOR SOLUTION in 1 CARTON (49884-905-64)
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": "883f5ee2-2d94-4fd7-9838-d4b572c9e0c3", "openfda": {"upc": ["0349884905644"], "unii": ["L4D5UA6CB4"], "rxcui": ["859063"], "spl_set_id": ["2d45648f-cbea-41a4-8e3e-007b7bb7912c"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 POWDER, FOR SOLUTION in 1 CARTON (49884-905-64)", "package_ndc": "49884-905-64", "marketing_start_date": "20230103"}], "brand_name": "Diclofenac Potassium", "product_id": "49884-905_883f5ee2-2d94-4fd7-9838-d4b572c9e0c3", "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": "49884-905", "generic_name": "Diclofenac Potassium", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA202964", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}