Package 31722-588-34

{"route": ["ORAL"], "spl_id": "103af555-44dd-5dfb-e063-6294a90a259f", "openfda": {"upc": ["0331722585309", "0331722588300", "0331722587303", "0331722586306"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["202d5142-6180-4d48-9a9f-1bd6992fc49b"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-588-01)", "package_ndc": "31722-588-01", "marketing_start_date": "20210917"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (31722-588-30)", "package_ndc": "31722-588-30", "marketing_start_date": "20210917"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-588-32)  / 10 TABLET in 1 BLISTER PACK (31722-588-31)", "package_ndc": "31722-588-32", "marketing_start_date": "20210917"}, {"sample": false, "description": "18 BLISTER PACK in 1 CARTON (31722-588-34)  / 7 TABLET in 1 BLISTER PACK (31722-588-33)", "package_ndc": "31722-588-34", "marketing_start_date": "20210917"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (31722-588-90)", "package_ndc": "31722-588-90", "marketing_start_date": "20210917"}], "brand_name": "Nebivolol", "product_id": "31722-588_103af555-44dd-5dfb-e063-6294a90a259f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "31722-588", "generic_name": "Nebivolol", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203825", "marketing_category": "ANDA", "marketing_start_date": "20210917", "listing_expiration_date": "20261231"}