cyclophosphamide
Generic: cyclophosphamide
Labeler: bamboo us bidco lccDrug Facts
Product Profile
Brand Name
cyclophosphamide
Generic Name
cyclophosphamide
Labeler
bamboo us bidco lcc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cyclophosphamide 500 mg/25mL
Manufacturer
Identifiers & Regulatory
Product NDC
83703-549
Product ID
83703-549_450da59c-b50e-4de0-e063-6394a90a0559
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
83703549
Hyphenated Format
83703-549
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 (83703-549-01) / 25 mL in 1 VIAL, SINGLE-DOSE (83703-549-25)
Packages (1)
Ingredients (1)
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 (83703-549-01) / 25 mL in 1 VIAL, SINGLE-DOSE (83703-549-25)", "package_ndc": "83703-549-01", "marketing_start_date": "20080521"}], "brand_name": "CYCLOPHOSPHAMIDE", "product_id": "83703-549_450da59c-b50e-4de0-e063-6394a90a0559", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "83703-549", "generic_name": "cyclophosphamide", "labeler_name": "Bamboo US Bidco LCC", "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"}