cyclophosphamide

Generic: cyclophosphamide

Labeler: sandoz inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclophosphamide
Generic Name cyclophosphamide
Labeler sandoz inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS ORAL
Active Ingredients

cyclophosphamide 1 g/50mL

Manufacturer
Sandoz Inc.

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
1734917 1734919 1734921
UPC
0307813233947 0307813244943 0307813255949
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 ANDA204555 (source: ndc)
Routes
INTRAVENOUS ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/50mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3244-94) / 50 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

cyclophosphamide (1 g/50mL)

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"}