Cyclophosphamide

Product NDC
0781-3255
11-digit product format
007813255
Labeler code
0781
Product ID
0781-3255_2f9d08d0-1f6c-0bf3-e063-6394a90a2b6f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
cyclophosphamide
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAVENOUS; ORAL
Labeler
Sandoz Inc.
Application
ANDA204555
Marketing category
ANDA
Marketing start
2014-10-31
Substance
CYCLOPHOSPHAMIDE
Active strength
2 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cyclophosphamide
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CYCLOPHOSPHAMIDE2 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii8N3DW7272P
Rxcui1734917, 1734919, 1734921

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0db1850b-2dc3-47a1-8b35-fab6e1685124Product name320250814
0b38b013-6fe7-0a7a-ece2-0a10ca467a97Product name420250801
f22fb018-dc36-4ffa-a765-94776b98899bProduct name120250620
e71baeca-a07a-452b-ba2b-50be55aedc79Product name220250617
913f6711-71c9-4a3d-a6d5-98cbd101b5d8Product name120231023
cd3d0a71-dbf2-4640-91f7-c99c45edfbb6Product name120231023
fbc3d08d-10bd-4e59-b59d-d530aede5badProduct name120220308

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0781-3255-94Cyclophosphamide100 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, FOR SOLUTION10011
0781-3255-94Cyclophosphamide1 in 1 CARTONINJECTION, POWDER, FOR SOLUTION111

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-3255-94EA - Each0781-325593a0418c-4dc5-4120-af16-caad9f32eee712014-12-01

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CYCLOPHOSPHAMIDEACTIVE INGREDIENT8N3DW7272PCYCLOPHOSPHAMIDE INJECTION, POWDER, FOR SOLUTION [SANDOZ INC.]3
CYCLOPHOSPHAMIDE ANHYDROUSACTIVE MOIETY6UXW23996MCYCLOPHOSPHAMIDE INJECTION, POWDER, FOR SOLUTION [SANDOZ INC.]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0781-3255CYCLOPHOSPHAMIDE INJECTION, POWDER, FOR SOLUTION [SANDOZ INC.]11Current NDC, Legacy NDC, 2 package rows20250308_0e9e22fa-178a-42fc-9f82-c303db3b245a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1734919cycloPHOSphamide 1 GM InjectionPSN0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734921cycloPHOSphamide 2 GM InjectionPSN0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734917cycloPHOSphamide 500 MG InjectionPSN0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734919cyclophosphamide 1000 MG InjectionSCD0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734921cyclophosphamide 2000 MG InjectionSCD0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734917cyclophosphamide 500 MG InjectionSCD0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734919cyclophosphamide (as cyclophosphamide monohydrate) 1000 MG InjectionSY0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734921cyclophosphamide (as cyclophosphamide monohydrate) 2000 MG InjectionSY0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734917cyclophosphamide (as cyclophosphamide monohydrate) 500 MG InjectionSY0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734919cyclophosphamide 1 GM InjectionSY0e9e22fa-178a-42fc-9f82-c303db3b245a11
1734921cyclophosphamide 2 GM InjectionSY0e9e22fa-178a-42fc-9f82-c303db3b245a11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0781-3255-94007813255941 VIAL, SINGLE-DOSE in 1 CARTON (0781-3255-94) / 100 mL in 1 VIAL, SINGLE-DOSE2014-10-310000-00-00NoNoCurrent