Package 0781-3529-10

Brand: cyclophosphamide

Generic: cyclophosphamide
NDC Package

Package Facts

Identity

Package NDC 0781-3529-10
Digits Only 0781352910
Product NDC 0781-3529
Product ID 0781-3529_3a7a4ad7-90ca-4d84-92f1-c61032067deb
Description

1 VIAL, MULTI-DOSE in 1 CARTON (0781-3529-10) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3529-70)

Marketing

Marketing Status
Marketed Since 2024-04-08
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"], "spl_id": "3a7a4ad7-90ca-4d84-92f1-c61032067deb", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["2679073"], "spl_set_id": ["cf2f4b95-0327-499a-a5a3-51b1bdef68c5"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0781-3529-10)  / 10 mL in 1 VIAL, MULTI-DOSE (0781-3529-70)", "package_ndc": "0781-3529-10", "marketing_start_date": "20240408"}], "brand_name": "Cyclophosphamide", "product_id": "0781-3529_3a7a4ad7-90ca-4d84-92f1-c61032067deb", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "product_ndc": "0781-3529", "generic_name": "Cyclophosphamide", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "1000 mg/10mL"}], "application_number": "NDA217150", "marketing_category": "NDA", "marketing_start_date": "20240408", "listing_expiration_date": "20261231"}