Package 46122-750-51

{"route": ["ORAL"], "spl_id": "335ad6a0-0537-b0e1-e063-6294a90a83b5", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["d1d94d37-4423-4914-9d86-c5ca6d5122f6"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["AMERISOURCE BERGEN"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (46122-750-51)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "46122-750-51", "marketing_start_date": "20230811"}], "brand_name": "Guaifenesin", "product_id": "46122-750_335ad6a0-0537-b0e1-e063-6294a90a83b5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "46122-750", "generic_name": "Guaifenesin", "labeler_name": "AMERISOURCE BERGEN", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA209254", "marketing_category": "ANDA", "marketing_start_date": "20230811", "listing_expiration_date": "20261231"}