Package 70518-3560-1

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 70518-3560-1
Digits Only 7051835601
Product NDC 70518-3560
Product ID 70518-3560_40ba2ee6-5b5c-a287-e063-6294a90a1d32
Description

5 POUCH in 1 CARTON (70518-3560-1) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-10-19
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": "40ba2ee6-5b5c-a287-e063-6294a90a1d32", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["0f9bf2c8-55c0-4b4d-97de-d6c7220c3862"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "5 POUCH in 1 CARTON (70518-3560-1)  / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "70518-3560-1", "marketing_start_date": "20221019"}], "brand_name": "Albuterol Sulfate", "product_id": "70518-3560_40ba2ee6-5b5c-a287-e063-6294a90a1d32", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-3560", "generic_name": "albuterol sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": ".83 mg/mL"}], "application_number": "ANDA207857", "marketing_category": "ANDA", "marketing_start_date": "20221019", "listing_expiration_date": "20261231"}