Package 0781-3233-94

Brand: cyclophosphamide

Generic: cyclophosphamide
NDC Package

Package Facts

Identity

Package NDC 0781-3233-94
Digits Only 0781323394
Product NDC 0781-3233
Product ID 0781-3233_2f9d08d0-1f6c-0bf3-e063-6394a90a2b6f
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3233-94) / 25 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2014-10-31
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": "2f9d08d0-1f6c-0bf3-e063-6394a90a2b6f", "openfda": {"upc": ["0307813233947", "0307813244943", "0307813255949"], "unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["0e9e22fa-178a-42fc-9f82-c303db3b245a"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3233-94)  / 25 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0781-3233-94", "marketing_start_date": "20141031"}], "brand_name": "Cyclophosphamide", "product_id": "0781-3233_2f9d08d0-1f6c-0bf3-e063-6394a90a2b6f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "0781-3233", "generic_name": "cyclophosphamide", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "500 mg/25mL"}], "application_number": "ANDA204555", "marketing_category": "ANDA", "marketing_start_date": "20141031", "listing_expiration_date": "20261231"}