Package 11822-0021-4

{"route": ["ORAL"], "spl_id": "5b8e52d1-e70e-41ca-99ae-c9eb4a9687df", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["0834bda9-e793-ad67-7f71-d2ffce47e5fc"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (11822-0021-4)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-0021-4", "marketing_start_date": "20230331"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (11822-0021-6)  / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-0021-6", "marketing_start_date": "20230723"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "11822-0021_5b8e52d1-e70e-41ca-99ae-c9eb4a9687df", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "11822-0021", "generic_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "Rite Aid Corporation", "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": "ANDA215434", "marketing_category": "ANDA", "marketing_start_date": "20220331", "listing_expiration_date": "20261231"}