Package 71872-7054-1

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 71872-7054-1
Digits Only 7187270541
Product NDC 71872-7054
Product ID 71872-7054_fceb313f-3623-ea34-e053-6294a90ab46d
Description

1 AMPULE in 1 BAG (71872-7054-1) / 3 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2018-03-06
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": "fceb313f-3623-ea34-e053-6294a90ab46d", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["6a4b4b95-d1d3-9051-e053-2a91aa0a52e8"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 AMPULE in 1 BAG (71872-7054-1)  / 3 mL in 1 AMPULE", "package_ndc": "71872-7054-1", "marketing_start_date": "20180306"}], "brand_name": "Albuterol Sulfate", "product_id": "71872-7054_fceb313f-3623-ea34-e053-6294a90ab46d", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "71872-7054", "generic_name": "Albuterol Sulfate", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/3mL"}], "application_number": "ANDA077839", "marketing_category": "ANDA", "marketing_start_date": "20111205", "listing_expiration_date": "20261231"}