Package 68016-995-03

{"route": ["ORAL"], "spl_id": "9cb9fb1e-0d5d-763a-4950-4b0d53a5b9ee", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["d1d8d0ec-2bdd-fb07-a051-d6353e3c240c"], "manufacturer_name": ["Chain Drug Consortium, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68016-995-03)  / 30 TABLET in 1 BOTTLE", "package_ndc": "68016-995-03", "marketing_start_date": "20140401"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (68016-995-45)  / 45 TABLET in 1 BOTTLE", "package_ndc": "68016-995-45", "marketing_start_date": "20140401"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "68016-995_9cb9fb1e-0d5d-763a-4950-4b0d53a5b9ee", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68016-995", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Chain Drug Consortium, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20140401", "listing_expiration_date": "20261231"}