| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 78670-050-03 | 78670-050 | HUMAN PRESCRIPTION DRUG | Lucemyra | lofexidine hydrochloride | TABLET, FILM COATED | ORAL | 20210209 | N/A | NDA | NDA209229 | USWM, LLC | LOFEXIDINE HYDROCHLORIDE | .2 mg/1 | 1 BOTTLE in 1 CARTON (78670-050-03) / 36 TABLET, FILM COATED in 1 BOTTLE |
| 78670-050-36 | 78670-050 | HUMAN PRESCRIPTION DRUG | Lucemyra | lofexidine hydrochloride | TABLET, FILM COATED | ORAL | 20210209 | N/A | NDA | NDA209229 | USWM, LLC | LOFEXIDINE HYDROCHLORIDE | .2 mg/1 | 1 BOTTLE in 1 CARTON (78670-050-36) / 36 TABLET, FILM COATED in 1 BOTTLE |
| 78670-050-96 | 78670-050 | HUMAN PRESCRIPTION DRUG | Lucemyra | lofexidine hydrochloride | TABLET, FILM COATED | ORAL | 20210209 | N/A | NDA | NDA209229 | USWM, LLC | LOFEXIDINE HYDROCHLORIDE | .2 mg/1 | 1 BOTTLE in 1 CARTON (78670-050-96) / 96 TABLET, FILM COATED in 1 BOTTLE |