Package 62559-721-01

Brand: terbutaline sulfate

Generic: terbutaline sulfate
NDC Package

Package Facts

Identity

Package NDC 62559-721-01
Digits Only 6255972101
Product NDC 62559-721
Product ID 62559-721_ee722f8c-05d6-43bc-825d-9496579032c4
Description

100 TABLET in 1 BOTTLE (62559-721-01)

Marketing

Marketing Status
Marketed Since 2018-10-16
Brand terbutaline sulfate
Generic terbutaline sulfate
Sample Package No

Linked Drug Pages (1)

Terbutaline Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ee722f8c-05d6-43bc-825d-9496579032c4", "openfda": {"upc": ["0362559721011", "0362559722018"], "unii": ["576PU70Y8E"], "rxcui": ["857677", "857683"], "spl_set_id": ["d810a15b-3e10-4f6c-a36e-8ddecbaba9c3"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62559-721-01)", "package_ndc": "62559-721-01", "marketing_start_date": "20181016"}], "brand_name": "Terbutaline Sulfate", "product_id": "62559-721_ee722f8c-05d6-43bc-825d-9496579032c4", "dosage_form": "TABLET", "product_ndc": "62559-721", "generic_name": "Terbutaline Sulfate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbutaline Sulfate", "active_ingredients": [{"name": "TERBUTALINE SULFATE", "strength": "2.5 mg/1"}], "application_number": "NDA017849", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20181016", "listing_expiration_date": "20261231"}