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=ANDA205300"
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
42708-005-30 42708-005 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA205300 QPharma, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-005-30)
0093-5058-10 0093-5058 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA205300 Teva Pharmaceuticals USA, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0093-5058-10)
0093-5058-98 0093-5058 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20170504 N/A ANDA ANDA205300 Teva Pharmaceuticals USA, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0093-5058-98)
42708-003-30 42708-003 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA205300 QPharma, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-003-30)
0093-5056-10 0093-5056 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA205300 Teva Pharmaceuticals USA, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0093-5056-10)
0093-5056-98 0093-5056 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20170504 N/A ANDA ANDA205300 Teva Pharmaceuticals USA, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0093-5056-98)
42708-004-30 42708-004 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20180531 N/A ANDA ANDA205300 QPharma, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-004-30)
0093-5057-05 0093-5057 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA205300 Teva Pharmaceuticals USA, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 80 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (0093-5057-05)
0093-5057-98 0093-5057 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20170504 N/A ANDA ANDA205300 Teva Pharmaceuticals USA, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0093-5057-98)
71205-098-30 71205-098 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20180904 N/A ANDA ANDA205300 Proficient Rx LP ATORVASTATIN CALCIUM TRIHYDRATE 80 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-098-30)
71205-098-60 71205-098 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20180904 N/A ANDA ANDA205300 Proficient Rx LP ATORVASTATIN CALCIUM TRIHYDRATE 80 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-098-60)
71205-098-90 71205-098 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20180904 N/A ANDA ANDA205300 Proficient Rx LP ATORVASTATIN CALCIUM TRIHYDRATE 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-098-90)
0093-5059-10 0093-5059 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20220523 N/A ANDA ANDA205300 Teva Pharmaceuticals USA, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0093-5059-10)
0093-5059-98 0093-5059 HUMAN PRESCRIPTION DRUG Atorvastatin Calcium Atorvastatin Calcium TABLET, FILM COATED ORAL 20170504 N/A ANDA ANDA205300 Teva Pharmaceuticals USA, Inc. ATORVASTATIN CALCIUM TRIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0093-5059-98)
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