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=ANDA204946"
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
70771-1168-3 70771-1168 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Lifesciences Limited FESOTERODINE FUMARATE 4 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1168-3)
70771-1168-4 70771-1168 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Lifesciences Limited FESOTERODINE FUMARATE 4 mg/1 10 BLISTER PACK in 1 CARTON (70771-1168-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1168-2)
70771-1168-9 70771-1168 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Lifesciences Limited FESOTERODINE FUMARATE 4 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1168-9)
70771-1169-3 70771-1169 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Lifesciences Limited FESOTERODINE FUMARATE 8 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-3)
70771-1169-4 70771-1169 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Lifesciences Limited FESOTERODINE FUMARATE 8 mg/1 10 BLISTER PACK in 1 CARTON (70771-1169-4) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70771-1169-2)
70771-1169-9 70771-1169 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Lifesciences Limited FESOTERODINE FUMARATE 8 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1169-9)
68382-479-06 68382-479 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Pharmaceuticals USA Inc. FESOTERODINE FUMARATE 4 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-479-06)
68382-479-16 68382-479 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Pharmaceuticals USA Inc. FESOTERODINE FUMARATE 4 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-479-16)
68382-479-77 68382-479 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Pharmaceuticals USA Inc. FESOTERODINE FUMARATE 4 mg/1 10 BLISTER PACK in 1 CARTON (68382-479-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-479-30)
68382-480-06 68382-480 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Pharmaceuticals USA Inc. FESOTERODINE FUMARATE 8 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-480-06)
68382-480-16 68382-480 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Pharmaceuticals USA Inc. FESOTERODINE FUMARATE 8 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-480-16)
68382-480-77 68382-480 HUMAN PRESCRIPTION DRUG fesoterodine fumarate fesoterodine fumarate TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171207 N/A ANDA ANDA204946 Zydus Pharmaceuticals USA Inc. FESOTERODINE FUMARATE 8 mg/1 10 BLISTER PACK in 1 CARTON (68382-480-77) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68382-480-30)
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