Package 70518-4490-0

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 70518-4490-0
Digits Only 7051844900
Product NDC 70518-4490
Product ID 70518-4490_407d27eb-478a-0456-e063-6294a90ac3a1
Description

5 POUCH in 1 CARTON (70518-4490-0) / 5 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-10-03
Brand albuterol sulfate
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "407d27eb-478a-0456-e063-6294a90ac3a1", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["54172384-9726-4a11-901e-3fb8f1baccae"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "5 POUCH in 1 CARTON (70518-4490-0)  / 5 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70518-4490-0", "marketing_start_date": "20251003"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "70518-4490_407d27eb-478a-0456-e063-6294a90ac3a1", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-4490", "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": "ANDA206224", "marketing_category": "ANDA", "marketing_start_date": "20251003", "listing_expiration_date": "20261231"}