cyclophosphamide

Generic: cyclophosphamide

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclophosphamide
Generic Name cyclophosphamide
Labeler bluepoint laboratories
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS ORAL
Active Ingredients

cyclophosphamide 1 g/50mL

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-443
Product ID 68001-443_4a9e24ce-e6fc-6f07-e063-6394a90ab4bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040745
Listing Expiration 2027-12-31
Marketing Start 2020-10-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001443
Hyphenated Format 68001-443

Supplemental Identifiers

RxCUI
1734917 1734919 1734921
UPC
0368001443272 0368001444323
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 ANDA040745 (source: ndc)
Routes
INTRAVENOUS ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/50mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-443-27) / 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": "4a9e24ce-e6fc-6f07-e063-6394a90ab4bd", "openfda": {"upc": ["0368001443272", "0368001444323"], "unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["d7e97b99-83db-42d0-8521-b87fe6467a67"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (68001-443-27)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68001-443-27", "marketing_start_date": "20201019"}], "brand_name": "Cyclophosphamide", "product_id": "68001-443_4a9e24ce-e6fc-6f07-e063-6394a90ab4bd", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "68001-443", "generic_name": "cyclophosphamide", "labeler_name": "BluePoint Laboratories", "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": "20201019", "listing_expiration_date": "20271231"}