Package 41415-995-30

{"route": ["ORAL"], "spl_id": "aac48a0b-2b28-4c14-9baa-84c08713e6c2", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["75236b23-af51-40b6-ad1b-f62a27093a16"], "manufacturer_name": ["PUBLIX SUPER MARKETS, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (41415-995-20)  / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "41415-995-20", "marketing_start_date": "20211108"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (41415-995-30)  / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "41415-995-30", "marketing_start_date": "20211108"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "41415-995_aac48a0b-2b28-4c14-9baa-84c08713e6c2", "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": "41415-995", "generic_name": "fexofenadine hydrochloride and pseudoephedrine hydrochloride", "labeler_name": "PUBLIX SUPER MARKETS, 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": "20211108", "listing_expiration_date": "20261231"}