Package 68382-183-05

{"route": ["ORAL"], "spl_id": "8692aee8-7eb4-4cbb-8a31-3ecc49660195", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["14fd7c1c-778e-46d4-9024-89b319f15f39"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-183-05)", "package_ndc": "68382-183-05", "marketing_start_date": "20140503"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-183-10)", "package_ndc": "68382-183-10", "marketing_start_date": "20140503"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68382-183-14)", "package_ndc": "68382-183-14", "marketing_start_date": "20140503"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68382-183-77)  / 1 TABLET in 1 BLISTER PACK (68382-183-30)", "package_ndc": "68382-183-77", "marketing_start_date": "20140503"}], "brand_name": "Buspirone hydrochloride", "product_id": "68382-183_8692aee8-7eb4-4cbb-8a31-3ecc49660195", "dosage_form": "TABLET", "product_ndc": "68382-183", "generic_name": "Buspirone hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20140503", "listing_expiration_date": "20261231"}