Package 81894-104-02

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 81894-104-02
Digits Only 8189410402
Product NDC 81894-104
Description

30 POUCH in 1 CARTON (81894-104-02) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2017-10-17
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": "2350a61a-3c03-d0f7-e063-6394a90ab78a", "openfda": {"upc": ["0381894104051", "0381894104303"], "unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["1810ff8e-d505-bf9c-e063-6394a90a6540"], "manufacturer_name": ["Luoxin Aurovitas Pharma (Chengdu) Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (81894-104-02)  / 1 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "81894-104-02", "marketing_start_date": "20171017"}, {"sample": false, "description": "5 POUCH in 1 CARTON (81894-104-25)  / 5 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "81894-104-25", "marketing_start_date": "20171017"}, {"sample": false, "description": "6 POUCH in 1 CARTON (81894-104-30)  / 5 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "81894-104-30", "marketing_start_date": "20171017"}, {"sample": false, "description": "12 POUCH in 1 CARTON (81894-104-60)  / 5 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "81894-104-60", "marketing_start_date": "20171017"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "81894-104_2350a61a-3c03-d0f7-e063-6394a90ab78a", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "81894-104", "generic_name": "ALBUTEROL SULFATE", "labeler_name": "Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.", "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": "20171017", "listing_expiration_date": "20261231"}