Package 21130-526-31

{"route": ["ORAL"], "spl_id": "5ef0c05a-40de-40cb-b52c-3f1ab96a5348", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["1092b8af-25f2-4c25-b3bc-5ffb14e96024"], "manufacturer_name": ["SAFEWAY INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-526-13)  / 120 TABLET in 1 BOTTLE", "package_ndc": "21130-526-13", "marketing_start_date": "20090606"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (21130-526-31)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "21130-526-31", "marketing_start_date": "20090606"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-526-38)  / 365 TABLET in 1 BOTTLE", "package_ndc": "21130-526-38", "marketing_start_date": "20090606"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-526-43)  / 45 TABLET in 1 BOTTLE", "package_ndc": "21130-526-43", "marketing_start_date": "20090606"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (21130-526-69)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "21130-526-69", "marketing_start_date": "20090606"}], "brand_name": "Loratadine", "product_id": "21130-526_5ef0c05a-40de-40cb-b52c-3f1ab96a5348", "dosage_form": "TABLET", "product_ndc": "21130-526", "generic_name": "Loratadine", "labeler_name": "SAFEWAY INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076134", "marketing_category": "ANDA", "marketing_start_date": "20090606", "listing_expiration_date": "20261231"}