Package 47335-613-88

{"route": ["ORAL"], "spl_id": "bc18daa3-5321-43bd-9d00-dabd9adac571", "openfda": {"nui": ["N0000175594", "M0014839"], "upc": ["0347335613810", "0347335614817", "0347335539813"], "unii": ["2679MF687A"], "rxcui": ["1098134", "1098141", "1098143"], "spl_set_id": ["8e290f96-e8c6-47fd-863f-1c9480f28d9b"], "pharm_class_cs": ["Nicotinic Acids [CS]"], "pharm_class_epc": ["Nicotinic Acid [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-08)", "package_ndc": "47335-613-08", "marketing_start_date": "20140627"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-18)", "package_ndc": "47335-613-18", "marketing_start_date": "20140627"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-81)", "package_ndc": "47335-613-81", "marketing_start_date": "20140627"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-83)", "package_ndc": "47335-613-83", "marketing_start_date": "20140627"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-88)", "package_ndc": "47335-613-88", "marketing_start_date": "20140627"}], "brand_name": "NIACIN", "product_id": "47335-613_bc18daa3-5321-43bd-9d00-dabd9adac571", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Nicotinic Acid [EPC]", "Nicotinic Acids [CS]"], "product_ndc": "47335-613", "generic_name": "NIACIN", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NIACIN", "active_ingredients": [{"name": "NIACIN", "strength": "1000 mg/1"}], "application_number": "ANDA200484", "marketing_category": "ANDA", "marketing_start_date": "20140627", "listing_expiration_date": "20261231"}