Package 47335-724-95

{"route": ["ORAL"], "spl_id": "554fd38b-a6cf-4b55-bfb2-ee7cb3ef48e8", "openfda": {"upc": ["0347335724837"], "unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["8afc0167-17bf-4ccd-91c9-8fb9c4e241c1"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (47335-724-64)  / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60)", "package_ndc": "47335-724-64", "marketing_start_date": "20180301"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (47335-724-66)  / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60)", "package_ndc": "47335-724-66", "marketing_start_date": "20180301"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (47335-724-75)  / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (47335-724-60)", "package_ndc": "47335-724-75", "marketing_start_date": "20180301"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-724-83)", "package_ndc": "47335-724-83", "marketing_start_date": "20180301"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (47335-724-94)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "47335-724-94", "marketing_start_date": "20180301"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (47335-724-95)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "47335-724-95", "marketing_start_date": "20180301"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (47335-724-99)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "47335-724-99", "marketing_start_date": "20180301"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "47335-724_554fd38b-a6cf-4b55-bfb2-ee7cb3ef48e8", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "47335-724", "generic_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA090818", "marketing_category": "ANDA", "marketing_start_date": "20180301", "listing_expiration_date": "20261231"}