| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 29300-152-16 | 29300-152 | HUMAN PRESCRIPTION DRUG | Quetiapine Fumarate | Quetiapine Fumarate | TABLET, FILM COATED | ORAL | 20160701 | N/A | ANDA | ANDA202674 | Unichem Pharmaceuticals (USA), Inc. | QUETIAPINE FUMARATE | 400 mg/1 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-152-16) |
| 0615-8568-39 | 0615-8568 | HUMAN PRESCRIPTION DRUG | Quetiapine Fumarate | Quetiapine Fumarate | TABLET, FILM COATED | ORAL | 20250218 | N/A | ANDA | ANDA202674 | NCS HealthCare of KY, LLC dba Vangard Labs | QUETIAPINE FUMARATE | 400 mg/1 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8568-39) |