cyclophosphamide

Generic: cyclophosphamide

Labeler: dr. reddy's labratories inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclophosphamide
Generic Name cyclophosphamide
Labeler dr. reddy's labratories inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cyclophosphamide anhydrous 200 mg/mL

Manufacturer
Dr. Reddy's Labratories Inc.

Identifiers & Regulatory

Product NDC 75907-190
Product ID 75907-190_81f6f0e0-48f4-4eb1-95e5-b1463e5f53f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA212501
Listing Expiration 2026-12-31
Marketing Start 2024-06-20

Pharmacologic Class

Established (EPC)
alkylating drug [epc]
Mechanism of Action
alkylating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 75907190
Hyphenated Format 75907-190

Supplemental Identifiers

RxCUI
2386859
UPC
0375907191022
UNII
6UXW23996M
NUI
N0000000236 N0000175558

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 NDA212501 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (75907-190-07) / 5 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

cyclophosphamide anhydrous (200 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "81f6f0e0-48f4-4eb1-95e5-b1463e5f53f5", "openfda": {"nui": ["N0000000236", "N0000175558"], "upc": ["0375907191022"], "unii": ["6UXW23996M"], "rxcui": ["2386859"], "spl_set_id": ["a5818647-d840-e9d7-c7b8-6541b485e44e"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Dr. Reddy's Labratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (75907-190-07)  / 5 mL in 1 VIAL", "package_ndc": "75907-190-07", "marketing_start_date": "20240620"}], "brand_name": "CYCLOPHOSPHAMIDE", "product_id": "75907-190_81f6f0e0-48f4-4eb1-95e5-b1463e5f53f5", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "75907-190", "generic_name": "cyclophosphamide", "labeler_name": "Dr. Reddy's Labratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOPHOSPHAMIDE", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE ANHYDROUS", "strength": "200 mg/mL"}], "application_number": "NDA212501", "marketing_category": "NDA", "marketing_start_date": "20240620", "listing_expiration_date": "20261231"}