Package 50090-6768-4

{"route": ["ORAL"], "spl_id": "fe1e72df-f70a-4e79-8ebf-10f3a9983961", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["5d37fc5a-7a2f-432e-b4e9-e00c246ce33c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6768-0)", "package_ndc": "50090-6768-0", "marketing_start_date": "20231023"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (50090-6768-1)", "package_ndc": "50090-6768-1", "marketing_start_date": "20231023"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6768-4)", "package_ndc": "50090-6768-4", "marketing_start_date": "20231023"}], "brand_name": "Diclofenac Potassium", "product_id": "50090-6768_fe1e72df-f70a-4e79-8ebf-10f3a9983961", "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": "50090-6768", "generic_name": "Diclofenac Potassium Tablets", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA215750", "marketing_category": "ANDA", "marketing_start_date": "20220512", "listing_expiration_date": "20261231"}