Package 71335-2936-1

{"route": ["ORAL"], "spl_id": "f8a739c5-2fac-409e-a788-85300bdad173", "openfda": {"nui": ["N0000020060", "N0000180187", "N0000175459"], "unii": ["QIC03ANI02"], "rxcui": ["198382"], "spl_set_id": ["d3faac3a-5c8c-4987-9703-c161fb29ec56"], "pharm_class_epc": ["Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]"], "pharm_class_moa": ["DNA Polymerase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2936-1)", "package_ndc": "71335-2936-1", "marketing_start_date": "20251028"}], "brand_name": "Famciclovir", "product_id": "71335-2936_f8a739c5-2fac-409e-a788-85300bdad173", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["DNA Polymerase Inhibitors [MoA]", "Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "71335-2936", "generic_name": "Famciclovir", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famciclovir", "active_ingredients": [{"name": "FAMCICLOVIR", "strength": "500 mg/1"}], "application_number": "ANDA201022", "marketing_category": "ANDA", "marketing_start_date": "20120113", "listing_expiration_date": "20261231"}