Package 68084-949-25

Brand: albuterol sulfate

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 68084-949-25
Digits Only 6808494925
Product NDC 68084-949
Product ID 68084-949_1e7d3421-f562-17f5-e063-6294a90a9358
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-949-25) / 1 TABLET in 1 BLISTER PACK (68084-949-95)

Marketing

Marketing Status
Marketed Since 2015-09-22
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": "1e7d3421-f562-17f5-e063-6294a90a9358", "openfda": {"unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["b0f73459-baeb-42a7-be48-2c3647d9b205"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-949-25)  / 1 TABLET in 1 BLISTER PACK (68084-949-95)", "package_ndc": "68084-949-25", "marketing_start_date": "20150922"}], "brand_name": "Albuterol Sulfate", "product_id": "68084-949_1e7d3421-f562-17f5-e063-6294a90a9358", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68084-949", "generic_name": "Albuterol Sulfate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/1"}], "application_number": "ANDA072637", "marketing_category": "ANDA", "marketing_start_date": "20150922", "listing_expiration_date": "20261231"}