Package 47335-756-52

{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "c9e56721-a62e-4703-8ea6-20bf51f244a6", "openfda": {"unii": ["021SEF3731", "J697UZ2A9J"], "rxcui": ["1437702"], "spl_set_id": ["38f9a201-3954-4370-8e71-7ec2df88a1ff"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POUCH in 1 CARTON (47335-756-49)  / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "47335-756-49", "marketing_start_date": "20211115"}, {"sample": false, "description": "12 POUCH in 1 CARTON (47335-756-52)  / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "47335-756-52", "marketing_start_date": "20211115"}], "brand_name": "Ipratropium Bromide and Albuterol Sulfate", "product_id": "47335-756_c9e56721-a62e-4703-8ea6-20bf51f244a6", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "47335-756", "generic_name": "Ipratropium Bromide and Albuterol Sulfate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ipratropium Bromide and Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/3mL"}, {"name": "IPRATROPIUM BROMIDE", "strength": ".5 mg/3mL"}], "application_number": "ANDA207875", "marketing_category": "ANDA", "marketing_start_date": "20211115", "listing_expiration_date": "20261231"}