Package 63323-665-01

Brand: terbutaline sulfate

Generic: terbutaline sulfate
NDC Package

Package Facts

Identity

Package NDC 63323-665-01
Digits Only 6332366501
Product NDC 63323-665
Description

25 VIAL, SINGLE-USE in 1 TRAY (63323-665-01) / 1 mL in 1 VIAL, SINGLE-USE (63323-665-00)

Marketing

Marketing Status
Marketed Since 2011-03-10
Brand terbutaline sulfate
Generic terbutaline sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "15846c75-dc60-4339-b97b-5c9d78d66cf1", "openfda": {"upc": ["0363323665005"], "unii": ["576PU70Y8E"], "rxcui": ["857635"], "spl_set_id": ["cec31032-f366-4524-9e01-63146e473b2b"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-USE in 1 TRAY (63323-665-01)  / 1 mL in 1 VIAL, SINGLE-USE (63323-665-00)", "package_ndc": "63323-665-01", "marketing_start_date": "20110310"}], "brand_name": "Terbutaline Sulfate", "product_id": "63323-665_15846c75-dc60-4339-b97b-5c9d78d66cf1", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "63323-665", "generic_name": "TERBUTALINE SULFATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbutaline Sulfate", "active_ingredients": [{"name": "TERBUTALINE SULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA076887", "marketing_category": "ANDA", "marketing_start_date": "20110310", "listing_expiration_date": "20261231"}