Package 71205-211-85
Brand: albuterol sulfate hfa
Generic: albuterol sulfatePackage Facts
Identity
Package NDC
71205-211-85
Digits Only
7120521185
Product NDC
71205-211
Description
1 INHALER in 1 CARTON (71205-211-85) / 200 AEROSOL, METERED in 1 INHALER
Marketing
Marketing Status
Brand
albuterol sulfate hfa
Generic
albuterol sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "3a369306-f46b-4a2c-bb6d-484f34bb0c43", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["d617e361-5c03-45ac-9bbe-0fa418edb19f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (71205-211-85) / 200 AEROSOL, METERED in 1 INHALER", "package_ndc": "71205-211-85", "marketing_start_date": "20190601"}], "brand_name": "Albuterol Sulfate HFA", "product_id": "71205-211_3a369306-f46b-4a2c-bb6d-484f34bb0c43", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "71205-211", "generic_name": "Albuterol Sulfate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "brand_name_suffix": "HFA", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "NDA021457", "marketing_category": "NDA", "marketing_start_date": "20190116", "listing_expiration_date": "20261231"}