Package 70752-102-12

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 70752-102-12
Digits Only 7075210212
Product NDC 70752-102
Product ID 70752-102_f8b35fdc-741f-4ebd-91d5-a55a7ef8e261
Description

473 mL in 1 BOTTLE (70752-102-12)

Marketing

Marketing Status
Marketed Since 2019-09-06
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": "f8b35fdc-741f-4ebd-91d5-a55a7ef8e261", "openfda": {"upc": ["0370752102124"], "unii": ["021SEF3731"], "rxcui": ["755497"], "spl_set_id": ["99a490cc-e41d-436b-9cf3-8facb7ac714f"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (70752-102-12)", "package_ndc": "70752-102-12", "marketing_start_date": "20190906"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "70752-102_f8b35fdc-741f-4ebd-91d5-a55a7ef8e261", "dosage_form": "SYRUP", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70752-102", "generic_name": "ALBUTEROL SULFATE", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "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": "20190906", "listing_expiration_date": "20261231"}