Package 72572-087-01

Brand: cyclophosphamide

Generic: cyclophosphamide
NDC Package

Package Facts

Identity

Package NDC 72572-087-01
Digits Only 7257208701
Product NDC 72572-087
Product ID 72572-087_474c3902-b6cc-4ee3-81e3-317e9bbcabcd
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (72572-087-01) / 25 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-12-14
Brand cyclophosphamide
Generic cyclophosphamide
Sample Package No

Linked Drug Pages (1)

Cyclophosphamide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS", "ORAL"], "spl_id": "474c3902-b6cc-4ee3-81e3-317e9bbcabcd", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["8627c83f-c057-495d-9f78-8b67bda97b3e"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72572-087-01)  / 25 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72572-087-01", "marketing_start_date": "20221214"}], "brand_name": "Cyclophosphamide", "product_id": "72572-087_474c3902-b6cc-4ee3-81e3-317e9bbcabcd", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "72572-087", "generic_name": "cyclophosphamide", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "500 mg/25mL"}], "application_number": "ANDA040745", "marketing_category": "ANDA", "marketing_start_date": "20080521", "listing_expiration_date": "20261231"}