Package 17270-0740-0

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 17270-0740-0
Digits Only 1727007400
Product NDC 17270-0740
Product ID 17270-0740_da039f76-a4c6-4463-a773-c433021a53e6
Description

1 INHALER in 1 CARTON (17270-0740-0) / 200 INHALANT in 1 INHALER

Marketing

Marketing Status
Marketed Since 2024-08-06
Brand albuterol sulfate
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "da039f76-a4c6-4463-a773-c433021a53e6", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["17858afa-dcdf-4612-b475-3b6baadfb639"], "manufacturer_name": ["Armstrong Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (17270-0740-0)  / 200 INHALANT in 1 INHALER", "package_ndc": "17270-0740-0", "marketing_start_date": "20240806"}], "brand_name": "Albuterol Sulfate", "product_id": "17270-0740_da039f76-a4c6-4463-a773-c433021a53e6", "dosage_form": "INHALANT", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "17270-0740", "generic_name": "Albuterol Sulfate", "labeler_name": "Armstrong Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA212447", "marketing_category": "ANDA", "marketing_start_date": "20240806", "listing_expiration_date": "20261231"}