Package 0115-2622-02

Brand: terbutaline sulfate

Generic: terbutaline sulfate
NDC Package

Package Facts

Identity

Package NDC 0115-2622-02
Digits Only 0115262202
Product NDC 0115-2622
Description

500 TABLET in 1 BOTTLE (0115-2622-02)

Marketing

Marketing Status
Marketed Since 2001-06-26
Brand terbutaline sulfate
Generic terbutaline sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "63142944-3083-4d47-908f-2984144b6c5d", "openfda": {"upc": ["0301152622011", "0301152611015"], "unii": ["576PU70Y8E"], "rxcui": ["857677", "857683"], "spl_set_id": ["382dcebb-6e41-4335-818d-b5822e3fb884"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0115-2622-01)", "package_ndc": "0115-2622-01", "marketing_start_date": "20010626"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0115-2622-02)", "package_ndc": "0115-2622-02", "marketing_start_date": "20010626"}], "brand_name": "TERBUTALINE SULFATE", "product_id": "0115-2622_63142944-3083-4d47-908f-2984144b6c5d", "dosage_form": "TABLET", "product_ndc": "0115-2622", "generic_name": "TERBUTALINE SULFATE", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TERBUTALINE SULFATE", "active_ingredients": [{"name": "TERBUTALINE SULFATE", "strength": "5 mg/1"}], "application_number": "ANDA075877", "marketing_category": "ANDA", "marketing_start_date": "20010626", "listing_expiration_date": "20261231"}