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=ANDA208682"
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
72789-080-10 72789-080 HUMAN PRESCRIPTION DRUG Moxifloxacin Hydrochloride Tablets, 400 mg Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED ORAL 20200410 N/A ANDA ANDA208682 PD-Rx Pharmaceuticals, Inc. MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE 400 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-080-10)
72205-001-05 72205-001 HUMAN PRESCRIPTION DRUG Moxifloxacin Hydrochloride Tablets, 400 mg Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED ORAL 20190416 N/A ANDA ANDA208682 Novadoz Pharmaceuticals LLC MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72205-001-05)
72205-001-30 72205-001 HUMAN PRESCRIPTION DRUG Moxifloxacin Hydrochloride Tablets, 400 mg Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED ORAL 20190416 N/A ANDA ANDA208682 Novadoz Pharmaceuticals LLC MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72205-001-30)
72205-001-31 72205-001 HUMAN PRESCRIPTION DRUG Moxifloxacin Hydrochloride Tablets, 400 mg Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED ORAL 20190416 N/A ANDA ANDA208682 Novadoz Pharmaceuticals LLC MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE 400 mg/1 50 BLISTER PACK in 1 CARTON (72205-001-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-001-11)
69539-006-05 69539-006 HUMAN PRESCRIPTION DRUG Moxifloxacin Hydrochloride Tablets, 400 mg Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED ORAL 20190416 N/A ANDA ANDA208682 MSN LABORATORIES PRIVATE LIMITED MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (69539-006-05)
69539-006-30 69539-006 HUMAN PRESCRIPTION DRUG Moxifloxacin Hydrochloride Tablets, 400 mg Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED ORAL 20190416 N/A ANDA ANDA208682 MSN LABORATORIES PRIVATE LIMITED MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69539-006-30)
69539-006-31 69539-006 HUMAN PRESCRIPTION DRUG Moxifloxacin Hydrochloride Tablets, 400 mg Moxifloxacin Hydrochloride Tablets, 400 mg TABLET, FILM COATED ORAL 20190416 N/A ANDA ANDA208682 MSN LABORATORIES PRIVATE LIMITED MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE 400 mg/1 50 BLISTER PACK in 1 CARTON (69539-006-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (69539-006-11)
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