Package 68788-7573-4

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68788-7573-4
Digits Only 6878875734
Product NDC 68788-7573
Product ID 68788-7573_e9b207d7-0c31-45ac-a0ab-8d5b96ffd983
Description

473 mL in 1 BOTTLE (68788-7573-4)

Marketing

Marketing Status
Marketed Since 2020-05-01
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": ["ORAL"], "spl_id": "e9b207d7-0c31-45ac-a0ab-8d5b96ffd983", "openfda": {"unii": ["021SEF3731"], "rxcui": ["755497"], "spl_set_id": ["4aafc2dd-744d-4726-828f-70355aee6f70"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (68788-7573-4)", "package_ndc": "68788-7573-4", "marketing_start_date": "20200501"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "68788-7573_e9b207d7-0c31-45ac-a0ab-8d5b96ffd983", "dosage_form": "SYRUP", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-7573", "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 mg/5mL"}], "application_number": "ANDA212197", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}