Package 76420-350-90

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 76420-350-90
Digits Only 7642035090
Product NDC 76420-350
Description

1 CANISTER in 1 CARTON (76420-350-90) / 200 AEROSOL, METERED in 1 CANISTER

Marketing

Marketing Status
Marketed Since 2025-05-07
Brand albuterol sulfate
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": "3485f152-2284-e5bd-e063-6394a90afa5b", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["264e2145-c7d4-4f4f-aa5b-9fe48a7c5b47"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (76420-350-90)  / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "76420-350-90", "marketing_start_date": "20250507"}], "brand_name": "Albuterol sulfate", "product_id": "76420-350_3485f152-2284-e5bd-e063-6394a90afa5b", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "76420-350", "generic_name": "Albuterol sulfate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA209954", "marketing_category": "ANDA", "marketing_start_date": "20200825", "listing_expiration_date": "20261231"}