Package 0904-7050-40

{"route": ["ORAL"], "spl_id": "33be2075-3e84-4738-af91-6f2f971cc0b4", "openfda": {"upc": ["0309047050406"], "unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["c34cda59-8a63-48ab-a19d-c06a1878f5da"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (0904-7050-40)", "package_ndc": "0904-7050-40", "marketing_end_date": "20261028", "marketing_start_date": "20191129"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0904-7050-60)", "package_ndc": "0904-7050-60", "marketing_end_date": "20261028", "marketing_start_date": "20191129"}], "brand_name": "Fexofenadine Hydrochloride", "product_id": "0904-7050_33be2075-3e84-4738-af91-6f2f971cc0b4", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0904-7050", "generic_name": "Fexofenadine HCl", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_end_date": "20261028", "marketing_start_date": "20191129"}