Package 68788-8492-2

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68788-8492-2
Digits Only 6878884922
Product NDC 68788-8492
Product ID 68788-8492_84a25c79-3c24-4979-b295-2495b90eb295
Description

5 POUCH in 1 CARTON (68788-8492-2) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-07-24
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": ["RESPIRATORY (INHALATION)"], "spl_id": "84a25c79-3c24-4979-b295-2495b90eb295", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["5de6a189-a8b7-4b33-b162-add6b6e4b275"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 POUCH in 1 CARTON (68788-8492-2)  / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "68788-8492-2", "marketing_start_date": "20230724"}], "brand_name": "Albuterol Sulfate", "product_id": "68788-8492_84a25c79-3c24-4979-b295-2495b90eb295", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-8492", "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": ".83 mg/mL"}], "application_number": "ANDA207857", "marketing_category": "ANDA", "marketing_start_date": "20230724", "listing_expiration_date": "20271231"}