cyclophosphamide

Generic: cyclophosphamide

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

Drug Facts

Product Profile

Brand Name cyclophosphamide
Generic Name cyclophosphamide
Labeler cipla usa inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cyclophosphamide 50 mg/1

Manufacturer
Cipla USA Inc.

Identifiers & Regulatory

Product NDC 69097-517
Product ID 69097-517_11c7b59d-18e5-4efb-bc77-5877d9b89bb1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211608
Listing Expiration 2026-12-31
Marketing Start 2019-01-18

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69097517
Hyphenated Format 69097-517

Supplemental Identifiers

RxCUI
1437968 1437969
UPC
0369097517076
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 ANDA211608 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (69097-517-07)
source: ndc

Packages (1)

69097-517-07 100 CAPSULE in 1 BOTTLE (69097-517-07)

Ingredients (1)

cyclophosphamide (50 mg/1)

Linked Drug Pages (1)

Cyclophosphamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "11c7b59d-18e5-4efb-bc77-5877d9b89bb1", "openfda": {"upc": ["0369097517076"], "unii": ["8N3DW7272P"], "rxcui": ["1437968", "1437969"], "spl_set_id": ["0e1cb955-99c8-4fe5-89d1-399c8e52174e"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (69097-517-07)", "package_ndc": "69097-517-07", "marketing_start_date": "20190118"}], "brand_name": "Cyclophosphamide", "product_id": "69097-517_11c7b59d-18e5-4efb-bc77-5877d9b89bb1", "dosage_form": "CAPSULE", "product_ndc": "69097-517", "generic_name": "Cyclophosphamide", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA211608", "marketing_category": "ANDA", "marketing_start_date": "20190118", "listing_expiration_date": "20261231"}