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=ANDA211797"
符合检索条件的记录共 10 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
70010-021-01 70010-021 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20201022 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 600 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-021-01)
70010-021-05 70010-021 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20201022 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 600 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-021-05)
70010-021-10 70010-021 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20210504 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 600 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-021-10)
70010-021-61 70010-021 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20220103 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 600 mg/1 3 BLISTER PACK in 1 CARTON (70010-021-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70010-021-62 70010-021 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20220103 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 600 mg/1 10 BLISTER PACK in 1 CARTON (70010-021-62) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70010-022-01 70010-022 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20201022 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-01)
70010-022-05 70010-022 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20201022 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-05)
70010-022-10 70010-022 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20210504 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-10)
70010-022-61 70010-022 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20220103 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 750 mg/1 3 BLISTER PACK in 1 CARTON (70010-022-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70010-022-62 70010-022 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20220103 N/A ANDA ANDA211797 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 750 mg/1 10 BLISTER PACK in 1 CARTON (70010-022-62) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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