cyclophosphamide

Generic: cyclophosphamide

Labeler: xgen pharmaceuticals djb, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclophosphamide
Generic Name cyclophosphamide
Labeler xgen pharmaceuticals djb, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS ORAL
Active Ingredients

cyclophosphamide 500 mg/25mL

Manufacturer
XGen Pharmaceuticals DJB, Inc.

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
1734917 1734919 1734921
UPC
0339822025510 0339822025015 0339822026012
UNII
8N3DW7272P

Packaging Origin

Original Packager
true

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
INTRAVENOUS ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/25mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (39822-0250-1) / 25 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

cyclophosphamide (500 mg/25mL)

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"}