Package 65219-200-05

Brand: temsirolimus

Generic: temsirolimus
NDC Package

Package Facts

Identity

Package NDC 65219-200-05
Digits Only 6521920005
Product NDC 65219-200
Description

1 KIT in 1 KIT (65219-200-05) * 1 mL in 1 VIAL, SINGLE-DOSE (65219-205-05) * 1.8 mL in 1 VIAL, SINGLE-DOSE (65219-202-05)

Marketing

Marketing Status
Marketed Since 2020-11-20
Brand temsirolimus
Generic temsirolimus
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2b33d5f1-198e-41ef-ac78-ccfd27fc137a", "openfda": {"rxcui": ["722289"], "spl_set_id": ["1c207bed-10e3-46f0-ad2c-69d5e5c97736"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (65219-200-05)  *  1 mL in 1 VIAL, SINGLE-DOSE (65219-205-05)  *  1.8 mL in 1 VIAL, SINGLE-DOSE (65219-202-05)", "package_ndc": "65219-200-05", "marketing_start_date": "20201120"}], "brand_name": "Temsirolimus", "product_id": "65219-200_2b33d5f1-198e-41ef-ac78-ccfd27fc137a", "dosage_form": "KIT", "product_ndc": "65219-200", "generic_name": "Temsirolimus", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Temsirolimus", "application_number": "ANDA207383", "marketing_category": "ANDA", "marketing_start_date": "20201120", "listing_expiration_date": "20261231"}