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=ANDA218372"
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
72789-534-01 72789-534 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251121 N/A ANDA ANDA218372 PD-Rx Pharmaceuticals, Inc. DEXAMETHASONE 4 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-534-01)
72888-235-01 72888-235 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251015 N/A ANDA ANDA218372 Advagen Pharma Ltd. DEXAMETHASONE .5 mg/1 100 TABLET in 1 BOTTLE (72888-235-01)
72888-236-01 72888-236 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251015 N/A ANDA ANDA218372 Advagen Pharma Ltd. DEXAMETHASONE .75 mg/1 100 TABLET in 1 BOTTLE (72888-236-01)
72888-237-01 72888-237 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251015 N/A ANDA ANDA218372 Advagen Pharma Ltd. DEXAMETHASONE 1 mg/1 100 TABLET in 1 BOTTLE (72888-237-01)
72888-238-01 72888-238 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251015 N/A ANDA ANDA218372 Advagen Pharma Ltd. DEXAMETHASONE 1.5 mg/1 100 TABLET in 1 BOTTLE (72888-238-01)
72888-239-01 72888-239 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251015 N/A ANDA ANDA218372 Advagen Pharma Ltd. DEXAMETHASONE 2 mg/1 100 TABLET in 1 BOTTLE (72888-239-01)
72888-240-01 72888-240 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251015 N/A ANDA ANDA218372 Advagen Pharma Ltd. DEXAMETHASONE 4 mg/1 100 TABLET in 1 BOTTLE (72888-240-01)
72789-534-95 72789-534 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251121 N/A ANDA ANDA218372 PD-Rx Pharmaceuticals, Inc. DEXAMETHASONE 4 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (72789-534-95)
72888-241-01 72888-241 HUMAN PRESCRIPTION DRUG DEXAMETHASONE DEXAMETHASONE TABLET ORAL 20251015 N/A ANDA ANDA218372 Advagen Pharma Ltd. DEXAMETHASONE 6 mg/1 100 TABLET in 1 BOTTLE (72888-241-01)
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