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=ANDA209036"
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
10702-192-01 10702-192 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 5 mg/1 100 TABLET in 1 BOTTLE (10702-192-01)
10702-192-03 10702-192 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE (10702-192-03)
10702-192-10 10702-192 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 5 mg/1 1000 TABLET in 1 BOTTLE (10702-192-10)
10702-192-50 10702-192 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 5 mg/1 500 TABLET in 1 BOTTLE (10702-192-50)
10702-193-01 10702-193 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 7.5 mg/1 100 TABLET in 1 BOTTLE (10702-193-01)
10702-193-03 10702-193 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 7.5 mg/1 30 TABLET in 1 BOTTLE (10702-193-03)
10702-193-10 10702-193 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 7.5 mg/1 1000 TABLET in 1 BOTTLE (10702-193-10)
10702-193-50 10702-193 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 7.5 mg/1 500 TABLET in 1 BOTTLE (10702-193-50)
10702-194-01 10702-194 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE (10702-194-01)
10702-194-03 10702-194 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE (10702-194-03)
10702-194-10 10702-194 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 10 mg/1 1000 TABLET in 1 BOTTLE (10702-194-10)
10702-194-50 10702-194 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20170622 N/A ANDA ANDA209036 KVK-Tech, Inc. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 10 mg/1 500 TABLET in 1 BOTTLE (10702-194-50)
70518-3491-0 70518-3491 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20220822 N/A ANDA ANDA209036 REMEDYREPACK INC. ACETAMINOPHEN; HYDROCODONE BITARTRATE 300 mg/1; 5 mg/1 100 POUCH in 1 BOX (70518-3491-0) / 1 TABLET in 1 POUCH (70518-3491-1)
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