Package 16714-858-01

Brand: cyclophosphamide

Generic: cyclophosphamide
NDC Package

Package Facts

Identity

Package NDC 16714-858-01
Digits Only 1671485801
Product NDC 16714-858
Product ID 16714-858_27e82150-4ad3-5be6-e063-6394a90a0e3f
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (16714-858-01) / 100 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2019-01-08
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", "ORAL"], "spl_id": "27e82150-4ad3-5be6-e063-6394a90a0e3f", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["1734917", "1734919", "1734921"], "spl_set_id": ["76f057be-e3da-0a89-e053-2a91aa0a8438"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (16714-858-01)  / 100 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "16714-858-01", "marketing_start_date": "20190108"}], "brand_name": "Cyclophosphamide", "product_id": "16714-858_27e82150-4ad3-5be6-e063-6394a90a0e3f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "product_ndc": "16714-858", "generic_name": "cyclophosphamide", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "2 g/100mL"}], "application_number": "ANDA204555", "marketing_category": "ANDA", "marketing_start_date": "20190108", "listing_expiration_date": "20261231"}