Package 70710-1061-1

Brand: albuterol

Generic: albuterol
NDC Package

Package Facts

Identity

Package NDC 70710-1061-1
Digits Only 7071010611
Product NDC 70710-1061
Product ID 70710-1061_1d5b3219-efd5-4842-9b6e-2ea1874d0d4d
Description

100 TABLET in 1 BOTTLE (70710-1061-1)

Marketing

Marketing Status
Marketed Since 2020-10-23
Brand albuterol
Generic albuterol
Sample Package No

Linked Drug Pages (1)

Albuterol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d5b3219-efd5-4842-9b6e-2ea1874d0d4d", "openfda": {"unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["c3fa0068-fd12-45de-818e-e929fb45ba05"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1061-1)", "package_ndc": "70710-1061-1", "marketing_start_date": "20201023"}], "brand_name": "Albuterol", "product_id": "70710-1061_1d5b3219-efd5-4842-9b6e-2ea1874d0d4d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70710-1061", "generic_name": "Albuterol", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/1"}], "application_number": "ANDA208884", "marketing_category": "ANDA", "marketing_start_date": "20201023", "listing_expiration_date": "20261231"}