Package 70771-1512-5

{"route": ["ORAL"], "spl_id": "f4ea29a0-b1df-4ca8-9438-1f0300eb6d9d", "openfda": {"unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["a4709eea-e4a2-46e2-850f-1e6afca01893"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1512-1)", "package_ndc": "70771-1512-1", "marketing_start_date": "20201023"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1512-5)", "package_ndc": "70771-1512-5", "marketing_start_date": "20201023"}], "brand_name": "Albuterol", "product_id": "70771-1512_f4ea29a0-b1df-4ca8-9438-1f0300eb6d9d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70771-1512", "generic_name": "Albuterol", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "4 mg/1"}], "application_number": "ANDA208884", "marketing_category": "ANDA", "marketing_start_date": "20201023", "listing_expiration_date": "20261231"}