Package 83703-550-01

Brand: cyclophosphamide

Generic: cyclophosphamide
NDC Package

Package Facts

Identity

Package NDC 83703-550-01
Digits Only 8370355001
Product NDC 83703-550
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (83703-550-01) / 50 mL in 1 VIAL, SINGLE-DOSE (83703-550-50)

Marketing

Marketing Status
Marketed Since 2008-05-21
Brand cyclophosphamide
Generic cyclophosphamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "ORAL"], "spl_id": "450da59c-b50e-4de0-e063-6394a90a0559", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["2873b99a-830d-0a7b-e063-6394a90a4de7"], "manufacturer_name": ["Bamboo US Bidco LCC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (83703-550-01)  / 50 mL in 1 VIAL, SINGLE-DOSE (83703-550-50)", "package_ndc": "83703-550-01", "marketing_start_date": "20080521"}], "brand_name": "CYCLOPHOSPHAMIDE", "product_id": "83703-550_450da59c-b50e-4de0-e063-6394a90a0559", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "83703-550", "generic_name": "cyclophosphamide", "labeler_name": "Bamboo US Bidco LCC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOPHOSPHAMIDE", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "1 g/50mL"}], "application_number": "ANDA040745", "marketing_category": "ANDA", "marketing_start_date": "20080521", "listing_expiration_date": "20261231"}