Package 46122-700-71

{"route": ["ORAL"], "spl_id": "d97803b2-8d2a-42a1-9864-581cf86f698c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "04JA59TNSJ"], "rxcui": ["1304111"], "spl_set_id": ["63932e68-b09d-4500-bc1d-cfb2c267df1c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["AmerisourceBergen Drug Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (46122-700-71)  / 50 TABLET in 1 BOTTLE", "package_ndc": "46122-700-71", "marketing_start_date": "20220113"}], "brand_name": "GNP Mucus Relief PE", "product_id": "46122-700_d97803b2-8d2a-42a1-9864-581cf86f698c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "46122-700", "generic_name": "Guaifenesin/phenylephrine", "labeler_name": "AmerisourceBergen Drug Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GNP Mucus Relief", "brand_name_suffix": "PE", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}