cyclophosphamide
Generic: cyclophosphamide
Labeler: sandoz inc.Drug Facts
Product Profile
Brand Name
cyclophosphamide
Generic Name
cyclophosphamide
Labeler
sandoz inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cyclophosphamide 1 g/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-3244
Product ID
0781-3244_2f9d08d0-1f6c-0bf3-e063-6394a90a2b6f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204555
Listing Expiration
2026-12-31
Marketing Start
2014-10-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07813244
Hyphenated Format
0781-3244
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
ANDA204555 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/50mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3244-94) / 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": "2f9d08d0-1f6c-0bf3-e063-6394a90a2b6f", "openfda": {"upc": ["0307813233947", "0307813244943", "0307813255949"], "unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["0e9e22fa-178a-42fc-9f82-c303db3b245a"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3244-94) / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0781-3244-94", "marketing_start_date": "20141031"}], "brand_name": "Cyclophosphamide", "product_id": "0781-3244_2f9d08d0-1f6c-0bf3-e063-6394a90a2b6f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "0781-3244", "generic_name": "cyclophosphamide", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "1 g/50mL"}], "application_number": "ANDA204555", "marketing_category": "ANDA", "marketing_start_date": "20141031", "listing_expiration_date": "20261231"}