cyclophosphamide
Generic: cyclophosphamide
Labeler: xgen pharmaceuticals djb, inc.Drug Facts
Product Profile
Brand Name
cyclophosphamide
Generic Name
cyclophosphamide
Labeler
xgen pharmaceuticals djb, inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
cyclophosphamide 1 g/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
39822-0255
Product ID
39822-0255_29b88d00-eeea-7282-e063-6294a90a4024
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211757
Listing Expiration
2026-12-31
Marketing Start
2023-12-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
398220255
Hyphenated Format
39822-0255
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
cyclophosphamide (source: ndc)
Generic Name
cyclophosphamide (source: ndc)
Application Number
ANDA211757 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/50mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (39822-0255-1) / 50 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "ORAL"], "spl_id": "29b88d00-eeea-7282-e063-6294a90a4024", "openfda": {"upc": ["0339822025510", "0339822025015", "0339822026012"], "unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["02e64046-687d-449e-e063-6294a90a6c32"], "manufacturer_name": ["XGen Pharmaceuticals DJB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (39822-0255-1) / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "39822-0255-1", "marketing_start_date": "20231219"}], "brand_name": "CYCLOPHOSPHAMIDE", "product_id": "39822-0255_29b88d00-eeea-7282-e063-6294a90a4024", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "product_ndc": "39822-0255", "generic_name": "Cyclophosphamide", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOPHOSPHAMIDE", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "1 g/50mL"}], "application_number": "ANDA211757", "marketing_category": "ANDA", "marketing_start_date": "20231219", "listing_expiration_date": "20261231"}