美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA089903"
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
51662-1558-3 51662-1558 HUMAN PRESCRIPTION DRUG PROCHLORPERAZINE EDISYLATE PROCHLORPERAZINE EDISYLATE INJECTION INTRAMUSCULAR; INTRAVENOUS 20220615 N/A ANDA ANDA089903 HF Acquisition Co LLC, DBA HealthFirst PROCHLORPERAZINE EDISYLATE 5 mg/mL 25 POUCH in 1 CASE (51662-1558-3) / 1 VIAL in 1 POUCH (51662-1558-2) / 2 mL in 1 VIAL
0641-6135-25 0641-6135 HUMAN PRESCRIPTION DRUG Prochlorperazine Edisylate Prochlorperazine Edisylate INJECTION INTRAMUSCULAR; INTRAVENOUS 19890829 N/A ANDA ANDA089903 Hikma Pharmaceuticals USA Inc. PROCHLORPERAZINE EDISYLATE 5 mg/mL 25 VIAL in 1 CARTON (0641-6135-25) / 2 mL in 1 VIAL (0641-6135-01)
72572-580-25 72572-580 HUMAN PRESCRIPTION DRUG Prochlorperazine Edisylate Prochlorperazine Edisylate INJECTION INTRAMUSCULAR; INTRAVENOUS 20191118 N/A ANDA ANDA089903 Civica, Inc. PROCHLORPERAZINE EDISYLATE 5 mg/mL 25 VIAL in 1 CARTON (72572-580-25) / 2 mL in 1 VIAL (72572-580-01)
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