| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72205-246-42 | 72205-246 | HUMAN PRESCRIPTION DRUG | lofexidine hydrochloride | lofexidine hydrochloride | TABLET, FILM COATED | ORAL | 20250301 | N/A | ANDA | ANDA218699 | Novadoz Pharmaceuticals LLC | LOFEXIDINE HYDROCHLORIDE | .2 mg/1 | 1 BOTTLE in 1 CARTON (72205-246-42) / 36 TABLET, FILM COATED in 1 BOTTLE |
| 72205-246-43 | 72205-246 | HUMAN PRESCRIPTION DRUG | lofexidine hydrochloride | lofexidine hydrochloride | TABLET, FILM COATED | ORAL | 20250301 | N/A | ANDA | ANDA218699 | Novadoz Pharmaceuticals LLC | LOFEXIDINE HYDROCHLORIDE | .2 mg/1 | 1 BOTTLE in 1 CARTON (72205-246-43) / 96 TABLET, FILM COATED in 1 BOTTLE |