Package 50090-1203-0

{"route": ["ORAL"], "spl_id": "a0388348-fc41-4d13-81ad-d8f25cd154d9", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406", "997512"], "spl_set_id": ["705e1087-61cb-43c3-8675-f56626a1707b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-1203-0)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "50090-1203-0", "marketing_start_date": "20141128"}], "brand_name": "ALLEGRA-D", "product_id": "50090-1203_a0388348-fc41-4d13-81ad-d8f25cd154d9", "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": "50090-1203", "generic_name": "fexofenadine hydrochloride and pseudoephedrine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALLEGRA-D", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "NDA020786", "marketing_category": "NDA", "marketing_start_date": "20110303", "listing_expiration_date": "20261231"}