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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
16714-572-01 | 16714-572 | HUMAN PRESCRIPTION DRUG | leuprolide acetate | leuprolide acetate | KIT | 20220801 | 20240930 | ANDA | ANDA078885 | NorthStar RxLLC | 1 KIT in 1 CARTON (16714-572-01) * 1 VIAL, MULTI-DOSE in 1 CARTON (16714-540-01) / 2.8 mL in 1 VIAL, MULTI-DOSE * 28 PACKET in 1 CARTON / 1 mL in 1 PACKET | |||
47335-936-40 | 47335-936 | HUMAN PRESCRIPTION DRUG | leuprolide acetate | leuprolide acetate | KIT | 20141215 | N/A | ANDA | ANDA078885 | Sun Pharmaceutical Industries, Inc. | 1 KIT in 1 CARTON (47335-936-40) * 1 VIAL, MULTI-DOSE in 1 CARTON / 2.8 mL in 1 VIAL, MULTI-DOSE * 1 mL in 1 PACKET |