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)
产品NDC71335-0232
产品类型HUMAN PRESCRIPTION DRUG
商品名PHENYTOIN SODIUM
通用名PHENYTOIN SODIUM
剂型CAPSULE, EXTENDED RELEASE
给药途径ORAL
市场类别ANDA
申请号ANDA040621
标签持有者Bryant Ranch Prepack
活性成分PHENYTOIN SODIUM
规格100 mg/1
药学分类Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]
DEA计划编号N/A
上市认证有效期20241231
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产品NDCNDC包装代码包装描述开始上市日期结束上市日期NDC号状态是否样品包装药品说明书
71335-023271335-0232-1100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0232-1) 20130730有效药品说明书及标签信息
71335-023271335-0232-230 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0232-2) 20130730有效药品说明书及标签信息
71335-023271335-0232-3180 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0232-3) 20130730有效药品说明书及标签信息
71335-023271335-0232-490 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0232-4) 20130730有效药品说明书及标签信息
71335-023271335-0232-5120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0232-5) 20130730有效药品说明书及标签信息
71335-023271335-0232-660 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0232-6) 20130730有效药品说明书及标签信息
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