| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 62135-632-90 | 62135-632 | HUMAN PRESCRIPTION DRUG | CIMETIDINE | CIMETIDINE | TABLET, FILM COATED | ORAL | 20230815 | N/A | ANDA | ANDA074329 | Chartwell RX, LLC | CIMETIDINE | 400 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-632-90) |
| 62135-631-90 | 62135-631 | HUMAN PRESCRIPTION DRUG | CIMETIDINE | CIMETIDINE | TABLET, FILM COATED | ORAL | 20230815 | N/A | ANDA | ANDA074329 | Chartwell RX, LLC | CIMETIDINE | 300 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-631-90) |
| 62135-633-90 | 62135-633 | HUMAN PRESCRIPTION DRUG | CIMETIDINE | CIMETIDINE | TABLET, FILM COATED | ORAL | 20230815 | N/A | ANDA | ANDA074329 | Chartwell RX, LLC | CIMETIDINE | 800 mg/1 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-633-90) |
| 62135-630-30 | 62135-630 | HUMAN PRESCRIPTION DRUG | CIMETIDINE | CIMETIDINE | TABLET, FILM COATED | ORAL | 20230815 | N/A | ANDA | ANDA074329 | Chartwell RX, LLC | CIMETIDINE | 200 mg/1 | 30 TABLET, FILM COATED in 1 BOTTLE (62135-630-30) |