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=ANDA200958"
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
69367-255-01 69367-255 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20200720 N/A ANDA ANDA200958 Westminster Pharmaceuticals, LLC METHOCARBAMOL 500 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-255-01)
69367-255-05 69367-255 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20200720 N/A ANDA ANDA200958 Westminster Pharmaceuticals, LLC METHOCARBAMOL 500 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-255-05)
35561-211-12 35561-211 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20181009 N/A ANDA ANDA200958 AustarPharma LLC METHOCARBAMOL 750 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-211-12)
35561-211-13 35561-211 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20181009 N/A ANDA ANDA200958 AustarPharma LLC METHOCARBAMOL 750 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-211-13)
0276-0510-10 0276-0510 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20220913 N/A ANDA ANDA200958 Misemer Pharmaceutical METHOCARBAMOL 1000 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0276-0510-10)
71205-019-30 71205-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA200958 Proficient Rx LP METHOCARBAMOL 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-019-30)
71205-019-40 71205-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA200958 Proficient Rx LP METHOCARBAMOL 500 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71205-019-40)
71205-019-45 71205-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA200958 Proficient Rx LP METHOCARBAMOL 500 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71205-019-45)
71205-019-60 71205-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA200958 Proficient Rx LP METHOCARBAMOL 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-019-60)
71205-019-90 71205-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA200958 Proficient Rx LP METHOCARBAMOL 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-019-90)
71205-019-20 71205-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA200958 Proficient Rx LP METHOCARBAMOL 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-019-20)
35561-349-12 35561-349 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20220716 N/A ANDA ANDA200958 AustarPharma LLC METHOCARBAMOL 1000 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-349-12)
35561-349-13 35561-349 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20220716 N/A ANDA ANDA200958 AustarPharma LLC METHOCARBAMOL 1000 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-349-13)
69367-256-01 69367-256 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20200720 N/A ANDA ANDA200958 Westminster Pharmaceuticals, LLC METHOCARBAMOL 750 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-256-01)
69367-256-05 69367-256 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20200720 N/A ANDA ANDA200958 Westminster Pharmaceuticals, LLC METHOCARBAMOL 750 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-256-05)
35561-212-12 35561-212 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20181010 N/A ANDA ANDA200958 AustarPharma LLC METHOCARBAMOL 500 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-12)
35561-212-13 35561-212 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20181010 N/A ANDA ANDA200958 AustarPharma LLC METHOCARBAMOL 500 mg/1 500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-13)
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