Package 70518-3442-0

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 70518-3442-0
Digits Only 7051834420
Product NDC 70518-3442
Product ID 70518-3442_3a99a020-a809-56ec-e063-6394a90a4dd9
Description

1 POUCH in 1 CARTON (70518-3442-0) / 25 AMPULE in 1 POUCH / 3 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2022-06-23
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": "3a99a020-a809-56ec-e063-6394a90a4dd9", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["aa3a49f3-667a-4897-a1b7-f067d025a93c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (70518-3442-0)  / 25 AMPULE in 1 POUCH / 3 mL in 1 AMPULE", "package_ndc": "70518-3442-0", "marketing_start_date": "20220623"}], "brand_name": "Albuterol Sulfate", "product_id": "70518-3442_3a99a020-a809-56ec-e063-6394a90a4dd9", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-3442", "generic_name": "Albuterol Sulfate", "labeler_name": "REMEDYREPACK 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": "20220623", "listing_expiration_date": "20261231"}