Package 43598-650-11

Brand: thiotepa

Generic: thiotepa
NDC Package

Package Facts

Identity

Package NDC 43598-650-11
Digits Only 4359865011
Product NDC 43598-650
Product ID 43598-650_e880a370-00f9-f7c7-a992-64756718360b
Description

1 VIAL in 1 CARTON (43598-650-11) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-05-04
Brand thiotepa
Generic thiotepa
Sample Package No

Linked Drug Pages (1)

Thiotepa ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRACAVITARY", "INTRAVENOUS", "INTRAVESICAL"], "spl_id": "e880a370-00f9-f7c7-a992-64756718360b", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["905Z5W3GKH"], "rxcui": ["1660009"], "spl_set_id": ["0def6a5e-4bf5-b1fd-47b7-0f17ecfd9bc2"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Dr.Reddy's Laboratories Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (43598-650-11)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "43598-650-11", "marketing_start_date": "20180504"}], "brand_name": "Thiotepa", "product_id": "43598-650_e880a370-00f9-f7c7-a992-64756718360b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "43598-650", "generic_name": "Thiotepa", "labeler_name": "Dr.Reddy's Laboratories Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiotepa", "active_ingredients": [{"name": "THIOTEPA", "strength": "15 mg/1"}], "application_number": "ANDA210337", "marketing_category": "ANDA", "marketing_start_date": "20180504", "listing_expiration_date": "20261231"}