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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
68071-3463-6 | 68071-3463 | HUMAN PRESCRIPTION DRUG | QUETIAPINE FUMARATE | QUETIAPINE FUMARATE | TABLET, EXTENDED RELEASE | ORAL | 20230719 | N/A | ANDA | ANDA206252 | NuCare Pharmaceuticals,Inc. | QUETIAPINE FUMARATE | 50 mg/1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3463-6) |
68001-511-06 | 68001-511 | HUMAN PRESCRIPTION DRUG | QUETIAPINE FUMARATE | QUETIAPINE FUMARATE | TABLET, EXTENDED RELEASE | ORAL | 20210831 | N/A | ANDA | ANDA206252 | Bluepoint Laboratories | QUETIAPINE FUMARATE | 50 mg/1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-511-06) |
16729-132-12 | 16729-132 | HUMAN PRESCRIPTION DRUG | QUETIAPINE FUMARATE | QUETIAPINE FUMARATE | TABLET, EXTENDED RELEASE | ORAL | 20171130 | N/A | ANDA | ANDA206252 | Accord Healthcare Inc. | QUETIAPINE FUMARATE | 50 mg/1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-132-12) |