Package 0363-2110-20

{"route": ["ORAL"], "spl_id": "4f95c9cf-97d7-4cb3-a78a-5e3e91e86550", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["1ed05c85-7a1c-440d-a5d7-e229528cedcd"], "manufacturer_name": ["walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0363-2110-20)", "package_ndc": "0363-2110-20", "marketing_start_date": "20180417"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0363-2110-30)", "package_ndc": "0363-2110-30", "marketing_start_date": "20180417"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "0363-2110_4f95c9cf-97d7-4cb3-a78a-5e3e91e86550", "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": "0363-2110", "generic_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "walgreens", "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": "20180417", "listing_expiration_date": "20261231"}