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 500 mg/25mL
Manufacturer
Identifiers & Regulatory
Product NDC
39822-0250
Product ID
39822-0250_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
398220250
Hyphenated Format
39822-0250
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
- 500 mg/25mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (39822-0250-1) / 25 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 (39822-0250-1) / 25 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "39822-0250-1", "marketing_start_date": "20231219"}], "brand_name": "CYCLOPHOSPHAMIDE", "product_id": "39822-0250_29b88d00-eeea-7282-e063-6294a90a4024", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "product_ndc": "39822-0250", "generic_name": "Cyclophosphamide", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOPHOSPHAMIDE", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "500 mg/25mL"}], "application_number": "ANDA211757", "marketing_category": "ANDA", "marketing_start_date": "20231219", "listing_expiration_date": "20261231"}