美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SUMYCIN"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
SUMYCIN 060429 001 ANDA TETRACYCLINE HYDROCHLORIDE CAPSULE;ORAL 250MG No No 1954/09/17 Approved Prior to Jan 1, 1982 APOTHECON Discontinued
SUMYCIN 060429 002 ANDA TETRACYCLINE HYDROCHLORIDE CAPSULE;ORAL 100MG No No 1954/09/17 Approved Prior to Jan 1, 1982 APOTHECON Discontinued
SUMYCIN 060429 003 ANDA TETRACYCLINE HYDROCHLORIDE CAPSULE;ORAL 500MG No No 1954/09/17 Approved Prior to Jan 1, 1982 APOTHECON Discontinued
SUMYCIN 060429 004 ANDA TETRACYCLINE HYDROCHLORIDE CAPSULE;ORAL 125MG No No 1954/09/17 Approved Prior to Jan 1, 1982 APOTHECON Discontinued
SUMYCIN 060400 001 ANDA TETRACYCLINE HYDROCHLORIDE SUSPENSION;ORAL 125MG/5ML No No 1957/06/21 Approved Prior to Jan 1, 1982 PAR PHARM Discontinued
SUMYCIN 061147 001 ANDA TETRACYCLINE HYDROCHLORIDE TABLET;ORAL 250MG No No 1971/02/10 Approved Prior to Jan 1, 1982 PAR PHARM Discontinued
SUMYCIN 061147 002 ANDA TETRACYCLINE HYDROCHLORIDE TABLET;ORAL 100MG No No 1971/02/10 Approved Prior to Jan 1, 1982 PAR PHARM Discontinued
SUMYCIN 061147 003 ANDA TETRACYCLINE HYDROCHLORIDE TABLET;ORAL 50MG No No 1971/02/10 Approved Prior to Jan 1, 1982 PAR PHARM Discontinued
SUMYCIN 061147 004 ANDA TETRACYCLINE HYDROCHLORIDE TABLET;ORAL 500MG No No 1971/02/10 Approved Prior to Jan 1, 1982 PAR PHARM Discontinued
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