Package 65219-133-20

Brand: cyclophosphamide

Generic: cyclophosphamide
NDC Package

Package Facts

Identity

Package NDC 65219-133-20
Digits Only 6521913320
Product NDC 65219-133
Product ID 65219-133_fadfc813-11a5-415a-9d70-06c579e7619c
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (65219-133-20) / 100 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2023-11-17
Brand cyclophosphamide
Generic cyclophosphamide
Sample Package No

Linked Drug Pages (1)

Cyclophosphamide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS", "ORAL"], "spl_id": "fadfc813-11a5-415a-9d70-06c579e7619c", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["31986d36-a1bf-4903-93a4-ce7386241ba1"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (65219-133-20)  / 100 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "65219-133-20", "marketing_start_date": "20231117"}], "brand_name": "Cyclophosphamide", "product_id": "65219-133_fadfc813-11a5-415a-9d70-06c579e7619c", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "65219-133", "generic_name": "cyclophosphamide", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "2 g/100mL"}], "application_number": "ANDA204555", "marketing_category": "ANDA", "marketing_start_date": "20231117", "listing_expiration_date": "20261231"}