Package 0904-6796-10

{"route": ["ORAL"], "spl_id": "cab8eef9-3094-4824-a5a6-3e11cd06853c", "openfda": {"unii": ["4P3T9QF9NZ"], "rxcui": ["313566"], "spl_set_id": ["6a6533fd-0579-4059-ba87-aa399829a8b0"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6796-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6796-04", "marketing_start_date": "20160318"}, {"sample": false, "description": "20 BLISTER PACK in 1 CARTON (0904-6796-10)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6796-10", "marketing_start_date": "20160318"}], "brand_name": "Valganciclovir", "product_id": "0904-6796_cab8eef9-3094-4824-a5a6-3e11cd06853c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "DNA Polymerase Inhibitors [MoA]", "Nucleoside Analog Antiviral [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "0904-6796", "generic_name": "Valganciclovir", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valganciclovir", "active_ingredients": [{"name": "VALGANCICLOVIR HYDROCHLORIDE", "strength": "450 mg/1"}], "application_number": "ANDA205166", "marketing_category": "ANDA", "marketing_start_date": "20160318", "listing_expiration_date": "20261231"}