Package 10019-982-01
Brand: cyclophosphamide
Generic: cyclophosphamidePackage Facts
Identity
Package NDC
10019-982-01
Digits Only
1001998201
Product NDC
10019-982
Description
1 BOTTLE in 1 CARTON (10019-982-01) / 100 TABLET in 1 BOTTLE (10019-982-09)
Marketing
Marketing Status
Brand
cyclophosphamide
Generic
cyclophosphamide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "64432fde-275f-41de-a67c-2feb02b69321", "openfda": {"unii": ["8N3DW7272P"], "rxcui": ["197549", "197550"], "spl_set_id": ["769ded74-6186-40a8-8e44-ceff67287451"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (10019-982-01) / 100 TABLET in 1 BOTTLE (10019-982-09)", "package_ndc": "10019-982-01", "marketing_start_date": "20200807"}], "brand_name": "Cyclophosphamide", "product_id": "10019-982_64432fde-275f-41de-a67c-2feb02b69321", "dosage_form": "TABLET", "product_ndc": "10019-982", "generic_name": "Cyclophosphamide", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclophosphamide", "active_ingredients": [{"name": "CYCLOPHOSPHAMIDE", "strength": "25 mg/1"}], "application_number": "NDA012141", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200807", "listing_expiration_date": "20261231"}