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=ANDA203135"
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
76282-377-02 76282-377 HUMAN PRESCRIPTION DRUG Calcium Acetate Calcium Acetate CAPSULE ORAL 20140414 N/A ANDA ANDA203135 EXELAN PHARMACEUTICALS, INC. CALCIUM ACETATE 667 mg/1 200 CAPSULE in 1 BOTTLE (76282-377-02)
76282-377-60 76282-377 HUMAN PRESCRIPTION DRUG Calcium Acetate Calcium Acetate CAPSULE ORAL 20140414 N/A ANDA ANDA203135 EXELAN PHARMACEUTICALS, INC. CALCIUM ACETATE 667 mg/1 60 CAPSULE in 1 BOTTLE (76282-377-60)
69097-862-03 69097-862 HUMAN PRESCRIPTION DRUG Calcium Acetate Calcium Acetate CAPSULE ORAL 20160726 N/A ANDA ANDA203135 Cipla USA Inc., CALCIUM ACETATE 667 mg/1 60 CAPSULE in 1 BOTTLE (69097-862-03)
69097-862-83 69097-862 HUMAN PRESCRIPTION DRUG Calcium Acetate Calcium Acetate CAPSULE ORAL 20160726 N/A ANDA ANDA203135 Cipla USA Inc., CALCIUM ACETATE 667 mg/1 200 CAPSULE in 1 BOTTLE (69097-862-83)
0615-8364-39 0615-8364 HUMAN PRESCRIPTION DRUG Calcium Acetate Calcium Acetate CAPSULE ORAL 20201209 N/A ANDA ANDA203135 NCS HealthCare of KY, Inc dba Vangard Labs CALCIUM ACETATE 667 mg/1 30 CAPSULE in 1 BLISTER PACK (0615-8364-39)
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