| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 71335-3103-8 | 71335-3103 | HUMAN PRESCRIPTION DRUG | Acyclovir | Acyclovir | TABLET | ORAL | 20260316 | N/A | ANDA | ANDA210401 | Bryant Ranch Prepack | ACYCLOVIR | 400 mg/1 | 10 TABLET in 1 BOTTLE (71335-3103-8) |
| 71335-3103-9 | 71335-3103 | HUMAN PRESCRIPTION DRUG | Acyclovir | Acyclovir | TABLET | ORAL | 20260316 | N/A | ANDA | ANDA210401 | Bryant Ranch Prepack | ACYCLOVIR | 400 mg/1 | 40 TABLET in 1 BOTTLE (71335-3103-9) |
| 62135-019-50 | 62135-019 | HUMAN PRESCRIPTION DRUG | Acyclovir | Acyclovir | TABLET | ORAL | 20220701 | N/A | ANDA | ANDA210401 | Chartwell RX, LLC | ACYCLOVIR | 800 mg/1 | 50 TABLET in 1 BOTTLE (62135-019-50) |
| 67296-2162-2 | 67296-2162 | HUMAN PRESCRIPTION DRUG | Acyclovir | Acyclovir | TABLET | ORAL | 20230620 | N/A | ANDA | ANDA210401 | Redpharm Drug | ACYCLOVIR | 400 mg/1 | 20 TABLET in 1 BOTTLE (67296-2162-2) |