| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0781-2672-02 | 0781-2672 | HUMAN PRESCRIPTION DRUG | Calcium Acetate | Calcium Acetate | CAPSULE | ORAL | 20120314 | 20241231 | NDA AUTHORIZED GENERIC | NDA021160 | Sandoz Inc | CALCIUM ACETATE | 667 mg/1 | 200 CAPSULE in 1 BOTTLE (0781-2672-02) |
| 70518-2372-0 | 70518-2372 | HUMAN PRESCRIPTION DRUG | Calcium Acetate | Calcium Acetate | CAPSULE | ORAL | 20191021 | 20241231 | NDA AUTHORIZED GENERIC | NDA021160 | REMEDYREPACK INC. | CALCIUM ACETATE | 667 mg/1 | 30 CAPSULE in 1 BLISTER PACK (70518-2372-0) |
| 0781-2081-02 | 0781-2081 | HUMAN PRESCRIPTION DRUG | Calcium Acetate | Calcium Acetate | CAPSULE | ORAL | 20120314 | 20241231 | NDA AUTHORIZED GENERIC | NDA021160 | Sandoz Inc | CALCIUM ACETATE | 667 mg/1 | 200 CAPSULE in 1 BOTTLE (0781-2081-02) |