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=ANDA209312"
符合检索条件的记录共 111 条，共 6 页，当前第 5 页 ，可点击列名称排序
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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
70518-1738-6 70518-1738 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20230622 N/A ANDA ANDA209312 REMEDYREPACK INC. METHOCARBAMOL 750 mg/1 60 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-6)
70518-1738-7 70518-1738 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20220816 N/A ANDA ANDA209312 REMEDYREPACK INC. METHOCARBAMOL 750 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-7)
70518-1738-8 70518-1738 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20230111 N/A ANDA ANDA209312 REMEDYREPACK INC. METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-8)
70518-1738-9 70518-1738 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250331 N/A ANDA ANDA209312 REMEDYREPACK INC. METHOCARBAMOL 750 mg/1 15 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-9)
70518-1723-4 70518-1723 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20221017 N/A ANDA ANDA209312 REMEDYREPACK INC. METHOCARBAMOL 500 mg/1 30 TABLET, COATED in 1 BLISTER PACK (70518-1723-4)
70518-1723-6 70518-1723 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20241224 N/A ANDA ANDA209312 REMEDYREPACK INC. METHOCARBAMOL 500 mg/1 60 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-6)
63739-992-10 63739-992 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20210722 20260331 ANDA ANDA209312 McKesson Corporation dba SKY Packaging METHOCARBAMOL 750 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-992-10) / 10 TABLET, COATED in 1 BLISTER PACK
71205-068-20 71205-068 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180801 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 750 mg/1 20 TABLET, COATED in 1 BOTTLE (71205-068-20)
71205-068-60 71205-068 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180801 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 750 mg/1 60 TABLET, COATED in 1 BOTTLE (71205-068-60)
71205-068-90 71205-068 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180801 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 750 mg/1 90 TABLET, COATED in 1 BOTTLE (71205-068-90)
71205-068-30 71205-068 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180702 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE (71205-068-30)
71205-068-40 71205-068 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180702 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 750 mg/1 40 TABLET, COATED in 1 BOTTLE (71205-068-40)
71205-068-45 71205-068 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180801 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 750 mg/1 45 TABLET, COATED in 1 BOTTLE (71205-068-45)
71205-167-30 71205-167 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181201 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 500 mg/1 30 TABLET, COATED in 1 BOTTLE (71205-167-30)
71205-167-60 71205-167 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181201 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 500 mg/1 60 TABLET, COATED in 1 BOTTLE (71205-167-60)
71205-167-90 71205-167 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181201 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 500 mg/1 90 TABLET, COATED in 1 BOTTLE (71205-167-90)
76420-893-05 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 500 TABLET, COATED in 1 BOTTLE (76420-893-05)
76420-893-60 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 60 TABLET, COATED in 1 BOTTLE (76420-893-60)
76420-893-90 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 90 TABLET, COATED in 1 BOTTLE (76420-893-90)
76420-894-01 76420-894 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 100 TABLET, COATED in 1 BOTTLE (76420-894-01)
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