cyclophosphamide

Generic: cyclophosphamide

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name cyclophosphamide
Generic Name cyclophosphamide
Labeler baxter healthcare corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cyclophosphamide 25 mg/1

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 10019-982
Product ID 10019-982_64432fde-275f-41de-a67c-2feb02b69321
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA012141
Listing Expiration 2026-12-31
Marketing Start 2020-08-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10019982
Hyphenated Format 10019-982

Supplemental Identifiers

RxCUI
197549 197550
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 NDA012141 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (10019-982-01) / 100 TABLET in 1 BOTTLE (10019-982-09)
source: ndc

Packages (1)

10019-982-01 1 BOTTLE in 1 CARTON (10019-982-01) / 100 TABLET in 1 BOTTLE (10019-982-09)

Ingredients (1)

cyclophosphamide (25 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": "64432fde-275f-41de-a67c-2feb02b69321", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["197549", "197550"], "spl_set_id": ["769ded74-6186-40a8-8e44-ceff67287451"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (10019-982-01)  / 100 TABLET in 1 BOTTLE (10019-982-09)", "package_ndc": "10019-982-01", "marketing_start_date": "20200807"}], "brand_name": "Cyclophosphamide", "product_id": "10019-982_64432fde-275f-41de-a67c-2feb02b69321", "dosage_form": "TABLET", "product_ndc": "10019-982", "generic_name": "Cyclophosphamide", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "25 mg/1"}], "application_number": "NDA012141", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200807", "listing_expiration_date": "20261231"}