Package 68788-4041-2

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68788-4041-2
Digits Only 6878840412
Product NDC 68788-4041
Product ID 68788-4041_081b7bbb-6692-4512-b135-863b73bf30a5
Description

1 INHALER in 1 CARTON (68788-4041-2) / 200 INHALANT in 1 INHALER

Marketing

Marketing Status
Marketed Since 2025-10-13
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": "081b7bbb-6692-4512-b135-863b73bf30a5", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["081b7bbb-6692-4512-b135-863b73bf30a5"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (68788-4041-2)  / 200 INHALANT in 1 INHALER", "package_ndc": "68788-4041-2", "marketing_start_date": "20251013"}], "brand_name": "Albuterol Sulfate", "product_id": "68788-4041_081b7bbb-6692-4512-b135-863b73bf30a5", "dosage_form": "INHALANT", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-4041", "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": "ANDA212447", "marketing_category": "ANDA", "marketing_start_date": "20251013", "listing_expiration_date": "20261231"}