Package 0093-3174-31

Brand: albuterol sulfate hfa

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 0093-3174-31
Digits Only 0093317431
Product NDC 0093-3174
Description

1 INHALER in 1 CARTON (0093-3174-31) / 200 AEROSOL, METERED in 1 INHALER

Marketing

Marketing Status
Marketed Since 2019-01-16
Brand albuterol sulfate hfa
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "d9fc7dd4-8c8c-4c83-a6b7-02d984f4135b", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["7bb5b6dd-9105-4ee7-b205-ed79cf4b371b"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (0093-3174-31)  / 200 AEROSOL, METERED in 1 INHALER", "package_ndc": "0093-3174-31", "marketing_start_date": "20190116"}], "brand_name": "Albuterol Sulfate HFA", "product_id": "0093-3174_d9fc7dd4-8c8c-4c83-a6b7-02d984f4135b", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "0093-3174", "generic_name": "Albuterol Sulfate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "brand_name_suffix": "HFA", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "NDA021457", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190116", "listing_expiration_date": "20261231"}