Package 64980-442-01

Brand: albuterol

Generic: albuterol
NDC Package

Package Facts

Identity

Package NDC 64980-442-01
Digits Only 6498044201
Product NDC 64980-442
Product ID 64980-442_f3d2f709-6e2e-4c25-8069-52661dc76e2d
Description

100 TABLET in 1 BOTTLE (64980-442-01)

Marketing

Marketing Status
Marketed Since 2018-06-29
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": "f3d2f709-6e2e-4c25-8069-52661dc76e2d", "openfda": {"upc": ["0364980443500", "0364980443012"], "unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["40f3cdbc-c9ee-4a3c-8061-a44b9a1d035c"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-442-01)", "package_ndc": "64980-442-01", "marketing_start_date": "20180629"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (64980-442-50)", "package_ndc": "64980-442-50", "marketing_start_date": "20180629"}], "brand_name": "Albuterol", "product_id": "64980-442_f3d2f709-6e2e-4c25-8069-52661dc76e2d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "64980-442", "generic_name": "albuterol", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/1"}], "application_number": "ANDA207046", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}