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=ANDA208052"
符合检索条件的记录共 51 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
70771-1737-9 70771-1737 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Lifesciences Limited LURASIDONE HYDROCHLORIDE 80 mg/1 90 TABLET, COATED in 1 BOTTLE (70771-1737-9)
70771-1738-1 70771-1738 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Lifesciences Limited LURASIDONE HYDROCHLORIDE 120 mg/1 100 TABLET, COATED in 1 BOTTLE (70771-1738-1)
70771-1738-3 70771-1738 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Lifesciences Limited LURASIDONE HYDROCHLORIDE 120 mg/1 30 TABLET, COATED in 1 BOTTLE (70771-1738-3)
70771-1738-4 70771-1738 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Lifesciences Limited LURASIDONE HYDROCHLORIDE 120 mg/1 10 BLISTER PACK in 1 CARTON (70771-1738-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1738-2)
70771-1738-5 70771-1738 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Lifesciences Limited LURASIDONE HYDROCHLORIDE 120 mg/1 500 TABLET, COATED in 1 BOTTLE (70771-1738-5)
70771-1738-9 70771-1738 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Lifesciences Limited LURASIDONE HYDROCHLORIDE 120 mg/1 90 TABLET, COATED in 1 BOTTLE (70771-1738-9)
68382-859-01 68382-859 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 60 mg/1 100 TABLET, COATED in 1 BOTTLE (68382-859-01)
68382-859-05 68382-859 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 60 mg/1 500 TABLET, COATED in 1 BOTTLE (68382-859-05)
68382-859-06 68382-859 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 60 mg/1 30 TABLET, COATED in 1 BOTTLE (68382-859-06)
68382-859-16 68382-859 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 60 mg/1 90 TABLET, COATED in 1 BOTTLE (68382-859-16)
68382-859-77 68382-859 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 60 mg/1 100 BLISTER PACK in 1 CARTON (68382-859-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-859-30)
68382-965-05 68382-965 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 20 mg/1 500 TABLET, COATED in 1 BOTTLE (68382-965-05)
68382-965-06 68382-965 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 20 mg/1 30 TABLET, COATED in 1 BOTTLE (68382-965-06)
68382-965-16 68382-965 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 20 mg/1 90 TABLET, COATED in 1 BOTTLE (68382-965-16)
68382-965-77 68382-965 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 20 mg/1 100 BLISTER PACK in 1 CARTON (68382-965-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-965-30)
68382-965-01 68382-965 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 20 mg/1 100 TABLET, COATED in 1 BOTTLE (68382-965-01)
68382-966-01 68382-966 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 40 mg/1 100 TABLET, COATED in 1 BOTTLE (68382-966-01)
68382-966-05 68382-966 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 40 mg/1 500 TABLET, COATED in 1 BOTTLE (68382-966-05)
68382-966-06 68382-966 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230323 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 40 mg/1 30 TABLET, COATED in 1 BOTTLE (68382-966-06)
68382-966-16 68382-966 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, COATED ORAL 20230201 N/A ANDA ANDA208052 Zydus Pharmaceuticals USA Inc. LURASIDONE HYDROCHLORIDE 40 mg/1 90 TABLET, COATED in 1 BOTTLE (68382-966-16)
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