Package 0143-9292-01

Brand: thiotepa

Generic: thiotepa
NDC Package

Package Facts

Identity

Package NDC 0143-9292-01
Digits Only 0143929201
Product NDC 0143-9292
Description

1 VIAL in 1 BOX, UNIT-DOSE (0143-9292-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-09-29
Brand thiotepa
Generic thiotepa
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRACAVITARY", "INTRAVENOUS", "INTRAVESICAL"], "spl_id": "f18a13d2-83c0-42a1-8980-60b228c23ab9", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["905Z5W3GKH"], "rxcui": ["1660004"], "spl_set_id": ["9ae8063c-ba28-4da2-a94c-8e1a5f75e4b3"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (0143-9292-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0143-9292-01", "marketing_start_date": "20230929"}], "brand_name": "Thiotepa", "product_id": "0143-9292_f18a13d2-83c0-42a1-8980-60b228c23ab9", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "0143-9292", "generic_name": "Thiotepa", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiotepa", "active_ingredients": [{"name": "THIOTEPA", "strength": "100 mg/1"}], "application_number": "ANDA211755", "marketing_category": "ANDA", "marketing_start_date": "20230929", "listing_expiration_date": "20261231"}