Package 0074-0501-01

Brand: vyalev

Generic: foscarbidopa/foslevodopa
NDC Package

Package Facts

Identity

Package NDC 0074-0501-01
Digits Only 0074050101
Product NDC 0074-0501
Product ID 0074-0501_4c17adf8-afd2-43c7-8aca-59a2ca647f2a
Description

7 VIAL, SINGLE-DOSE in 1 CARTON (0074-0501-01) / 10 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-04-12
Brand vyalev
Generic foscarbidopa/foslevodopa
Sample Package No

Linked Drug Pages (1)

Vyalev ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "4c17adf8-afd2-43c7-8aca-59a2ca647f2a", "openfda": {"unii": ["5NT8HCA4OO", "37NQZ0J76I"], "rxcui": ["2695782", "2695789"], "spl_set_id": ["28e806e4-951c-40a9-9f0c-d0929caf054c"], "manufacturer_name": ["AbbVie Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 VIAL, SINGLE-DOSE in 1 CARTON (0074-0501-01)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0074-0501-01", "marketing_start_date": "20220412"}], "brand_name": "Vyalev", "product_id": "0074-0501_4c17adf8-afd2-43c7-8aca-59a2ca647f2a", "dosage_form": "INJECTION", "product_ndc": "0074-0501", "generic_name": "foscarbidopa/foslevodopa", "labeler_name": "AbbVie Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vyalev", "active_ingredients": [{"name": "FOSCARBIDOPA", "strength": "12 mg/mL"}, {"name": "FOSLEVODOPA", "strength": "240 mg/mL"}], "application_number": "NDA216962", "marketing_category": "NDA", "marketing_start_date": "20220412", "listing_expiration_date": "20261231"}