Package 68788-8878-2

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68788-8878-2
Digits Only 6878888782
Product NDC 68788-8878
Description

1 CANISTER in 1 CARTON (68788-8878-2) / 200 AEROSOL, METERED in 1 CANISTER

Marketing

Marketing Status
Marketed Since 2025-05-19
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": "99782bc8-56d9-41f8-935e-0d0de27f0c34", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["99782bc8-56d9-41f8-935e-0d0de27f0c34"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (68788-8878-2)  / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "68788-8878-2", "marketing_start_date": "20250519"}], "brand_name": "Albuterol sulfate", "product_id": "68788-8878_99782bc8-56d9-41f8-935e-0d0de27f0c34", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-8878", "generic_name": "Albuterol sulfate", "labeler_name": "Preferred Pharmaceuticals, 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": "20250519", "listing_expiration_date": "20261231"}