Package 10019-956-01

Brand: cyclophosphamide

Generic: cyclophosphamide
NDC Package

Package Facts

Identity

Package NDC 10019-956-01
Digits Only 1001995601
Product NDC 10019-956
Product ID 10019-956_2e97b53e-e39d-4190-9091-b8856a7cff7b
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (10019-956-01) / 50 mL in 1 VIAL, SINGLE-DOSE (10019-956-16)

Marketing

Marketing Status
Marketed Since 2008-05-21
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": "2e97b53e-e39d-4190-9091-b8856a7cff7b", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["591d9955-3d9c-4cdc-a308-2f1288376b9f"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (10019-956-01)  / 50 mL in 1 VIAL, SINGLE-DOSE (10019-956-16)", "package_ndc": "10019-956-01", "marketing_start_date": "20080521"}], "brand_name": "Cyclophosphamide", "product_id": "10019-956_2e97b53e-e39d-4190-9091-b8856a7cff7b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "10019-956", "generic_name": "cyclophosphamide", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "1 g/50mL"}], "application_number": "ANDA040745", "marketing_category": "ANDA", "marketing_start_date": "20080521", "listing_expiration_date": "20261231"}