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=ANDA040545"
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
55700-984-30 55700-984 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20220928 N/A ANDA ANDA040545 Quality Care Products, LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 30 TABLET in 1 BOTTLE (55700-984-30)
55700-984-60 55700-984 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20220928 N/A ANDA ANDA040545 Quality Care Products, LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 60 TABLET in 1 BOTTLE (55700-984-60)
55700-984-90 55700-984 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20220928 N/A ANDA ANDA040545 Quality Care Products, LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 90 TABLET in 1 BOTTLE (55700-984-90)
0406-0522-01 0406-0522 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20040630 N/A ANDA ANDA040545 SpecGx LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 100 TABLET in 1 BOTTLE (0406-0522-01)
0406-0522-05 0406-0522 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20040630 N/A ANDA ANDA040545 SpecGx LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 500 TABLET in 1 BOTTLE (0406-0522-05)
0406-0522-23 0406-0522 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20040630 N/A ANDA ANDA040545 SpecGx LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 1 TABLET in 1 BLISTER PACK (0406-0522-23)
0406-0522-62 0406-0522 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20040630 N/A ANDA ANDA040545 SpecGx LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 100 TABLET in 1 BLISTER PACK (0406-0522-62)
0406-0523-01 0406-0523 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20040630 N/A ANDA ANDA040545 SpecGx LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE (0406-0523-01)
0406-0523-05 0406-0523 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20040630 N/A ANDA ANDA040545 SpecGx LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 500 TABLET in 1 BOTTLE (0406-0523-05)
0406-0523-23 0406-0523 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20040630 N/A ANDA ANDA040545 SpecGx LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 1 TABLET in 1 BLISTER PACK (0406-0523-23)
0406-0523-62 0406-0523 HUMAN PRESCRIPTION DRUG OXYCODONE AND ACETAMINOPHEN oxycodone hydrochloride and acetaminophen TABLET ORAL 20040630 N/A ANDA ANDA040545 SpecGx LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BLISTER PACK (0406-0523-62)
72189-426-30 72189-426 HUMAN PRESCRIPTION DRUG Oxycodone/APAP Oxycodone/APAP TABLET ORAL 20230221 N/A ANDA ANDA040545 Direct_Rx ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE (72189-426-30)
72189-426-60 72189-426 HUMAN PRESCRIPTION DRUG Oxycodone/APAP Oxycodone/APAP TABLET ORAL 20230221 N/A ANDA ANDA040545 Direct_Rx ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 60 TABLET in 1 BOTTLE (72189-426-60)
72189-426-72 72189-426 HUMAN PRESCRIPTION DRUG Oxycodone/APAP Oxycodone/APAP TABLET ORAL 20230221 N/A ANDA ANDA040545 Direct_Rx ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 120 TABLET in 1 BOTTLE (72189-426-72)
72189-426-90 72189-426 HUMAN PRESCRIPTION DRUG Oxycodone/APAP Oxycodone/APAP TABLET ORAL 20230221 N/A ANDA ANDA040545 Direct_Rx ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 90 TABLET in 1 BOTTLE (72189-426-90)
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