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=ANDA219585"
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
31722-455-31 31722-455 HUMAN PRESCRIPTION DRUG ZINC SULFATE ZINC SULFATE INJECTION, SOLUTION INTRAVENOUS 20250501 N/A ANDA ANDA219585 Camber Pharmaceuticals, Inc. ZINC SULFATE 5 mg/mL 25 VIAL in 1 CARTON (31722-455-31) / 5 mL in 1 VIAL (31722-455-32)
31722-454-31 31722-454 HUMAN PRESCRIPTION DRUG ZINC SULFATE ZINC SULFATE INJECTION, SOLUTION INTRAVENOUS 20250501 N/A ANDA ANDA219585 Camber Pharmaceuticals, Inc. ZINC SULFATE 3 mg/mL 25 VIAL in 1 CARTON (31722-454-31) / 10 mL in 1 VIAL (31722-454-10)
31722-453-31 31722-453 HUMAN PRESCRIPTION DRUG ZINC SULFATE ZINC SULFATE INJECTION, SOLUTION INTRAVENOUS 20250501 N/A ANDA ANDA219585 Camber Pharmaceuticals, Inc. ZINC SULFATE 1 mg/mL 25 VIAL in 1 CARTON (31722-453-31) / 10 mL in 1 VIAL (31722-453-10)
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