Package 47335-903-61

{"route": ["ORAL"], "spl_id": "c8178883-9da2-4b4f-88ee-182d628a2e41", "openfda": {"upc": ["0347335907889", "0347335906882", "0347335905885", "0347335903881", "0347335904888"], "unii": ["2S3PL1B6UJ"], "rxcui": ["312743", "312744", "312745", "317174", "616483", "616487"], "spl_set_id": ["ffe52b98-9872-48c1-90fd-8fcd37c3432f"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (47335-903-18)", "package_ndc": "47335-903-18", "marketing_start_date": "20120328"}, {"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-903-61)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "47335-903-61", "marketing_start_date": "20120328"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-903-83)", "package_ndc": "47335-903-83", "marketing_start_date": "20120328"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-903-88)", "package_ndc": "47335-903-88", "marketing_start_date": "20120328"}], "brand_name": "Quetiapine fumarate", "product_id": "47335-903_c8178883-9da2-4b4f-88ee-182d628a2e41", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "47335-903", "generic_name": "Quetiapine fumarate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "ANDA201190", "marketing_category": "ANDA", "marketing_start_date": "20120328", "listing_expiration_date": "20261231"}