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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
CIMETIDINE HYDROCHLORIDE | 074757 | 001 | ANDA | CIMETIDINE HYDROCHLORIDE | SOLUTION;ORAL | EQ 300MG BASE/5ML | No | No | 1997/10/17 | 1997/10/17 | PHARMOBEDIENT CNSLTG | Discontinued |
CIMETIDINE HYDROCHLORIDE | 074664 | 001 | ANDA | CIMETIDINE HYDROCHLORIDE | SOLUTION;ORAL | EQ 300MG BASE/5ML | No | Yes | 1997/10/28 | 1997/10/28 | PAI HOLDINGS PHARM | Prescription |
CIMETIDINE HYDROCHLORIDE | 074252 | 001 | ANDA | CIMETIDINE HYDROCHLORIDE | INJECTABLE;INJECTION | EQ 300MG BASE/2ML | No | No | 1997/11/26 | 1997/11/26 | TEVA PARENTERAL | Discontinued |
CIMETIDINE HYDROCHLORIDE | 075110 | 001 | ANDA | CIMETIDINE HYDROCHLORIDE | SOLUTION;ORAL | EQ 300MG BASE/5ML | No | No | 1998/06/18 | 1998/06/18 | ANI PHARMS | Discontinued |
CIMETIDINE HYDROCHLORIDE | 074859 | 001 | ANDA | CIMETIDINE HYDROCHLORIDE | SOLUTION;ORAL | EQ 300MG BASE/5ML | No | No | 1998/07/09 | 1998/07/09 | ANI PHARMS | Discontinued |
CIMETIDINE HYDROCHLORIDE | 075560 | 001 | ANDA | CIMETIDINE HYDROCHLORIDE | SOLUTION;ORAL | EQ 300MG BASE/5ML | No | No | 2000/03/15 | 2000/03/15 | PHARM ASSOC | Discontinued |