美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA216355"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
72603-408-01 72603-408 HUMAN PRESCRIPTION DRUG Paclitaxel protein-bound particles for injectable suspension (albumin-bound) Paclitaxel INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION INTRAVENOUS 20250910 N/A ANDA ANDA216355 NorthStar Rx LLC PACLITAXEL 100 mg/20mL 1 VIAL, SINGLE-USE in 1 CARTON (72603-408-01) / 20 mL in 1 VIAL, SINGLE-USE
68001-651-37 68001-651 HUMAN PRESCRIPTION DRUG Paclitaxel protein-bound particles for injectable suspension (albumin-bound) Paclitaxel INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION INTRAVENOUS 20250718 N/A ANDA ANDA216355 BluePoint Laboratories PACLITAXEL 100 mg/20mL 1 VIAL, SINGLE-USE in 1 CARTON (68001-651-37) / 20 mL in 1 VIAL, SINGLE-USE
71288-183-50 71288-183 HUMAN PRESCRIPTION DRUG Paclitaxel protein-bound particles for injectable suspension (albumin-bound) Paclitaxel INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION INTRAVENOUS 20250515 N/A ANDA ANDA216355 Meitheal Pharmaceuticals Inc. PACLITAXEL 100 mg/20mL 1 VIAL, SINGLE-USE in 1 CARTON (71288-183-50) / 20 mL in 1 VIAL, SINGLE-USE
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