| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 0187-2049-30 | 0187-2049 | HUMAN PRESCRIPTION DRUG | Cardizem LA | Diltiazem Hydrochloride | TABLET, EXTENDED RELEASE | ORAL | 20101225 | N/A | NDA | NDA021392 | Bausch Health US LLC | DILTIAZEM HYDROCHLORIDE | 360 mg/1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-30) |
| 0187-2049-90 | 0187-2049 | HUMAN PRESCRIPTION DRUG | Cardizem LA | Diltiazem Hydrochloride | TABLET, EXTENDED RELEASE | ORAL | 20101225 | N/A | NDA | NDA021392 | Bausch Health US LLC | DILTIAZEM HYDROCHLORIDE | 360 mg/1 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-90) |
| 0187-2050-30 | 0187-2050 | HUMAN PRESCRIPTION DRUG | Cardizem LA | Diltiazem Hydrochloride | TABLET, EXTENDED RELEASE | ORAL | 20101225 | N/A | NDA | NDA021392 | Bausch Health US LLC | DILTIAZEM HYDROCHLORIDE | 420 mg/1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2050-30) |
| 0187-2050-90 | 0187-2050 | HUMAN PRESCRIPTION DRUG | Cardizem LA | Diltiazem Hydrochloride | TABLET, EXTENDED RELEASE | ORAL | 20101225 | N/A | NDA | NDA021392 | Bausch Health US LLC | DILTIAZEM HYDROCHLORIDE | 420 mg/1 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2050-90) |