Package 70710-1832-0

{"route": ["ORAL"], "spl_id": "47dd2b04-1417-2e67-e063-6294a90ae24b", "openfda": {"upc": ["0370710183202"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["1aa3d8d6-dd1c-46c7-96f9-2b5c9d72764a"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70710-1832-0)", "package_ndc": "70710-1832-0", "marketing_start_date": "20220512"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1832-1)", "package_ndc": "70710-1832-1", "marketing_start_date": "20220512"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70710-1832-5)", "package_ndc": "70710-1832-5", "marketing_start_date": "20220512"}], "brand_name": "Diclofenac Potassium", "product_id": "70710-1832_47dd2b04-1417-2e67-e063-6294a90ae24b", "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": "70710-1832", "generic_name": "Diclofenac Potassium Tablets", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "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": "20271231"}