| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 62135-336-90 | 62135-336 | HUMAN PRESCRIPTION DRUG | Diltiazem Hydrochloride | Diltiazem Hydrochloride | TABLET | ORAL | 20240617 | N/A | ANDA | ANDA074093 | Chartwell RX, LLC | DILTIAZEM HYDROCHLORIDE | 120 mg/1 | 90 TABLET in 1 BOTTLE (62135-336-90) |
| 62135-335-90 | 62135-335 | HUMAN PRESCRIPTION DRUG | Diltiazem Hydrochloride | Diltiazem Hydrochloride | TABLET | ORAL | 20240617 | N/A | ANDA | ANDA074093 | Chartwell RX, LLC | DILTIAZEM HYDROCHLORIDE | 90 mg/1 | 90 TABLET in 1 BOTTLE (62135-335-90) |
| 62135-334-12 | 62135-334 | HUMAN PRESCRIPTION DRUG | Diltiazem Hydrochloride | Diltiazem Hydrochloride | TABLET | ORAL | 20240617 | N/A | ANDA | ANDA074093 | Chartwell RX, LLC | DILTIAZEM HYDROCHLORIDE | 60 mg/1 | 120 TABLET in 1 BOTTLE (62135-334-12) |
| 62135-333-12 | 62135-333 | HUMAN PRESCRIPTION DRUG | Diltiazem Hydrochloride | Diltiazem Hydrochloride | TABLET | ORAL | 20240617 | N/A | ANDA | ANDA074093 | Chartwell RX, LLC | DILTIAZEM HYDROCHLORIDE | 30 mg/1 | 120 TABLET in 1 BOTTLE (62135-333-12) |