Package 64980-642-03

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 64980-642-03
Digits Only 6498064203
Product NDC 64980-642
Description

30 POUCH in 1 CARTON (64980-642-03) / 1 VIAL, SINGLE-DOSE in 1 POUCH / .5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-04-30
Brand albuterol sulfate
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "33015e7c-a4d2-ecac-e063-6394a90aae00", "openfda": {"unii": ["021SEF3731"], "rxcui": ["245314"], "spl_set_id": ["3236f82c-14e9-dfd4-e063-6294a90ac43d"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (64980-642-03)  / 1 VIAL, SINGLE-DOSE in 1 POUCH / .5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "64980-642-03", "marketing_start_date": "20250430"}], "brand_name": "Albuterol Sulfate", "product_id": "64980-642_33015e7c-a4d2-ecac-e063-6394a90aae00", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "64980-642", "generic_name": "Albuterol Sulfate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/.5mL"}], "application_number": "ANDA075664", "marketing_category": "ANDA", "marketing_start_date": "20250414", "listing_expiration_date": "20261231"}