Package 85742-007-06

{"route": ["ORAL"], "spl_id": "dc65647e-1905-4af9-8d6e-d64e0c0d8ee4", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0385742007068"], "unii": ["VZI5B1W380"], "rxcui": ["283536"], "spl_set_id": ["7be73d22-f87b-4459-a91c-37c1e34db230"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Kanchan Healthcare Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BOTTLE, GLASS (85742-007-06)", "package_ndc": "85742-007-06", "marketing_start_date": "20250501"}], "brand_name": "Oxcarbazepine", "product_id": "85742-007_dc65647e-1905-4af9-8d6e-d64e0c0d8ee4", "dosage_form": "SUSPENSION", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "85742-007", "generic_name": "Oxcarbazepine", "labeler_name": "Kanchan Healthcare Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "300 mg/5mL"}], "application_number": "ANDA217782", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}