cyclophosphamide
Generic: cyclophosphamide
Labeler: civica, inc.Drug Facts
Product Profile
Brand Name
cyclophosphamide
Generic Name
cyclophosphamide
Labeler
civica, inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cyclophosphamide 500 mg/25mL
Manufacturer
Identifiers & Regulatory
Product NDC
72572-087
Product ID
72572-087_474c3902-b6cc-4ee3-81e3-317e9bbcabcd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040745
Listing Expiration
2026-12-31
Marketing Start
2008-05-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72572087
Hyphenated Format
72572-087
Supplemental Identifiers
RxCUI
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
ANDA040745 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/25mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (72572-087-01) / 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": "474c3902-b6cc-4ee3-81e3-317e9bbcabcd", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["8627c83f-c057-495d-9f78-8b67bda97b3e"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72572-087-01) / 25 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72572-087-01", "marketing_start_date": "20221214"}], "brand_name": "Cyclophosphamide", "product_id": "72572-087_474c3902-b6cc-4ee3-81e3-317e9bbcabcd", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "72572-087", "generic_name": "cyclophosphamide", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "500 mg/25mL"}], "application_number": "ANDA040745", "marketing_category": "ANDA", "marketing_start_date": "20080521", "listing_expiration_date": "20261231"}