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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0781-5514-01 | 0781-5514 | HUMAN PRESCRIPTION DRUG | Griseofulvin | Griseofulvin | TABLET | ORAL | 20130807 | N/A | ANDA | ANDA091592 | Sandoz Inc | GRISEOFULVIN | 250 mg/1 | 100 TABLET in 1 BOTTLE (0781-5514-01) |
0781-5514-05 | 0781-5514 | HUMAN PRESCRIPTION DRUG | Griseofulvin | Griseofulvin | TABLET | ORAL | 20130807 | N/A | ANDA | ANDA091592 | Sandoz Inc | GRISEOFULVIN | 250 mg/1 | 500 TABLET in 1 BOTTLE (0781-5514-05) |
0781-5515-01 | 0781-5515 | HUMAN PRESCRIPTION DRUG | Griseofulvin | Griseofulvin | TABLET | ORAL | 20130807 | N/A | ANDA | ANDA091592 | Sandoz Inc | GRISEOFULVIN | 500 mg/1 | 100 TABLET in 1 BOTTLE (0781-5515-01) |
0781-5515-05 | 0781-5515 | HUMAN PRESCRIPTION DRUG | Griseofulvin | Griseofulvin | TABLET | ORAL | 20130807 | N/A | ANDA | ANDA091592 | Sandoz Inc | GRISEOFULVIN | 500 mg/1 | 500 TABLET in 1 BOTTLE (0781-5515-05) |