Package 68788-8399-2

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68788-8399-2
Digits Only 6878883992
Product NDC 68788-8399
Product ID 68788-8399_ff08ba3b-5da2-4a99-a931-72c24d5a1835
Description

25 AMPULE in 1 POUCH (68788-8399-2) / 3 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2023-03-01
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": "ff08ba3b-5da2-4a99-a931-72c24d5a1835", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["c90e80b2-882e-4c0c-bfac-d67eb1da724d"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 POUCH (68788-8399-2)  / 3 mL in 1 AMPULE", "package_ndc": "68788-8399-2", "marketing_start_date": "20230301"}], "brand_name": "Albuterol Sulfate", "product_id": "68788-8399_ff08ba3b-5da2-4a99-a931-72c24d5a1835", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-8399", "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": "2.5 mg/3mL"}], "application_number": "ANDA077839", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20271231"}