| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69842-037-35 | 69842-037 | HUMAN OTC DRUG | Acetaminophen | Acetaminophen | TABLET, EXTENDED RELEASE | ORAL | 20201223 | N/A | ANDA | ANDA207229 | CVS Pharmacy, Inc. | ACETAMINOPHEN | 650 mg/1 | 225 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-037-35) |
| 30142-157-35 | 30142-157 | HUMAN OTC DRUG | Acetaminophen | Acetaminophen | TABLET, EXTENDED RELEASE | ORAL | 20210525 | N/A | ANDA | ANDA207229 | KROGER COMPANY | ACETAMINOPHEN | 650 mg/1 | 225 TABLET, EXTENDED RELEASE in 1 BOTTLE (30142-157-35) |
| 30142-157-07 | 30142-157 | HUMAN OTC DRUG | Acetaminophen | Acetaminophen | TABLET, EXTENDED RELEASE | ORAL | 20210525 | N/A | ANDA | ANDA207229 | KROGER COMPANY | ACETAMINOPHEN | 650 mg/1 | 1 BOTTLE in 1 CARTON (30142-157-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE |