Package 69238-1345-1

Brand: albuterol

Generic: albuterol
NDC Package

Package Facts

Identity

Package NDC 69238-1345-1
Digits Only 6923813451
Product NDC 69238-1345
Product ID 69238-1345_d66ddd1b-c4f1-461d-b4ec-9362f4880e47
Description

100 TABLET in 1 BOTTLE (69238-1345-1)

Marketing

Marketing Status
Marketed Since 2018-05-24
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": "d66ddd1b-c4f1-461d-b4ec-9362f4880e47", "openfda": {"unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["230d66fc-f62c-42a6-adb3-0a0f879c8ad4"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69238-1345-1)", "package_ndc": "69238-1345-1", "marketing_start_date": "20180524"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69238-1345-5)", "package_ndc": "69238-1345-5", "marketing_start_date": "20180524"}], "brand_name": "Albuterol", "product_id": "69238-1345_d66ddd1b-c4f1-461d-b4ec-9362f4880e47", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "69238-1345", "generic_name": "Albuterol", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "4 mg/1"}], "application_number": "ANDA208804", "marketing_category": "ANDA", "marketing_start_date": "20180524", "listing_expiration_date": "20261231"}