Package 76420-531-01

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 76420-531-01
Digits Only 7642053101
Product NDC 76420-531
Product ID 76420-531_f104fd15-0d76-3db4-e053-2995a90a1a88
Description

200 AEROSOL, METERED in 1 CANISTER (76420-531-01)

Marketing

Marketing Status
Marketed Since 2022-12-13
Brand albuterol sulfate
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (1)

Albuterol Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "f104fd15-0d76-3db4-e053-2995a90a1a88", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123111"], "spl_set_id": ["87ff8be7-3a49-44bd-92de-eb8db24af95b"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "200 AEROSOL, METERED in 1 CANISTER (76420-531-01)", "package_ndc": "76420-531-01", "marketing_start_date": "20221213"}], "brand_name": "Albuterol Sulfate", "product_id": "76420-531_f104fd15-0d76-3db4-e053-2995a90a1a88", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "76420-531", "generic_name": "Albuterol Sulfate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA207085", "marketing_category": "ANDA", "marketing_start_date": "20211130", "listing_expiration_date": "20261231"}