Package 76204-028-60

{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "459fa0f5-35dd-d6e5-e063-6394a90a6f14", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831246"], "spl_set_id": ["0209cd6c-5c43-0b93-e063-6294a90ac964"], "manufacturer_name": ["Ritedose Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 CARTON (76204-028-60)  / 30 AMPULE in 1 POUCH (76204-028-12)  / 2 mL in 1 AMPULE", "package_ndc": "76204-028-60", "marketing_start_date": "20211201"}], "brand_name": "Cromolyn Sodium Inhalation Solution", "product_id": "76204-028_459fa0f5-35dd-d6e5-e063-6394a90a6f14", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "76204-028", "generic_name": "Cromolyn Sodium Inhalation Solution", "labeler_name": "Ritedose Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cromolyn Sodium Inhalation Solution", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "20 mg/2mL"}], "application_number": "ANDA209453", "marketing_category": "ANDA", "marketing_start_date": "20211201", "listing_expiration_date": "20261231"}