cyclophosphamide
Generic: cyclophosphamide
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
cyclophosphamide
Generic Name
cyclophosphamide
Labeler
baxter healthcare corporation
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cyclophosphamide 1 g/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
10019-956
Product ID
10019-956_2e97b53e-e39d-4190-9091-b8856a7cff7b
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
10019956
Hyphenated Format
10019-956
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
- 1 g/50mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (10019-956-01) / 50 mL in 1 VIAL, SINGLE-DOSE (10019-956-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "ORAL"], "spl_id": "2e97b53e-e39d-4190-9091-b8856a7cff7b", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["591d9955-3d9c-4cdc-a308-2f1288376b9f"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (10019-956-01) / 50 mL in 1 VIAL, SINGLE-DOSE (10019-956-16)", "package_ndc": "10019-956-01", "marketing_start_date": "20080521"}], "brand_name": "Cyclophosphamide", "product_id": "10019-956_2e97b53e-e39d-4190-9091-b8856a7cff7b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "10019-956", "generic_name": "cyclophosphamide", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "1 g/50mL"}], "application_number": "ANDA040745", "marketing_category": "ANDA", "marketing_start_date": "20080521", "listing_expiration_date": "20261231"}