Package 53041-234-47

{"route": ["ORAL"], "spl_id": "8186c3e8-1ae5-459d-8771-ad2d1ae95387", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621", "636522"], "spl_set_id": ["20f9e083-419d-429d-a570-24b312ed5d2a"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Guardian Drug Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (53041-234-37)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "53041-234-37", "marketing_start_date": "20180301"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (53041-234-47)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "53041-234-47", "marketing_start_date": "20180301"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (53041-234-58)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "53041-234-58", "marketing_start_date": "20180301"}], "brand_name": "Guaifenesin Extended-Release 1200 mg", "product_id": "53041-234_8186c3e8-1ae5-459d-8771-ad2d1ae95387", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "53041-234", "generic_name": "Guaifenesin", "labeler_name": "Guardian Drug Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin Extended-Release 1200 mg", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA209215", "marketing_category": "ANDA", "marketing_start_date": "20180301", "listing_expiration_date": "20261231"}