Package 10019-935-01

Brand: cyclophosphamide

Generic: cyclophosphamide
NDC Package

Package Facts

Identity

Package NDC 10019-935-01
Digits Only 1001993501
Product NDC 10019-935
Product ID 10019-935_b745f3eb-670e-494a-bc38-210549c8681e
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (10019-935-01) / 25 mL in 1 VIAL, SINGLE-DOSE (10019-935-25)

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": "b745f3eb-670e-494a-bc38-210549c8681e", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["6bae5c14-9e87-4fb6-ae9c-4d875c1ecffe"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (10019-935-01)  / 25 mL in 1 VIAL, SINGLE-DOSE (10019-935-25)", "package_ndc": "10019-935-01", "marketing_start_date": "20080521"}], "brand_name": "CYCLOPHOSPHAMIDE", "product_id": "10019-935_b745f3eb-670e-494a-bc38-210549c8681e", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "10019-935", "generic_name": "cyclophosphamide", "labeler_name": "Baxter Healthcare Corporation", "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"}