Package 59651-334-05

Brand: albuterol

Generic: albuterol
NDC Package

Package Facts

Identity

Package NDC 59651-334-05
Digits Only 5965133405
Product NDC 59651-334
Product ID 59651-334_f89dffb1-5c4b-48aa-90b4-74043fc9b690
Description

500 TABLET in 1 BOTTLE (59651-334-05)

Marketing

Marketing Status
Marketed Since 2020-05-14
Brand albuterol
Generic albuterol
Sample Package No

Linked Drug Pages (1)

Albuterol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f89dffb1-5c4b-48aa-90b4-74043fc9b690", "openfda": {"unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["ff9b287b-e4a4-4c12-ad2f-6b7d55b20dc6"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-334-01)", "package_ndc": "59651-334-01", "marketing_start_date": "20200514"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (59651-334-05)", "package_ndc": "59651-334-05", "marketing_start_date": "20200514"}], "brand_name": "Albuterol", "product_id": "59651-334_f89dffb1-5c4b-48aa-90b4-74043fc9b690", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "59651-334", "generic_name": "Albuterol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "4 mg/1"}], "application_number": "ANDA213657", "marketing_category": "ANDA", "marketing_start_date": "20200514", "listing_expiration_date": "20261231"}