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=ANDA210001"
符合检索条件的记录共 16 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
72189-088-03 72189-088 HUMAN PRESCRIPTION DRUG AZITHROMYCIN AZITHROMYCIN TABLET, FILM COATED ORAL 20200618 N/A ANDA ANDA210001 DIRECT RX AZITHROMYCIN DIHYDRATE 500 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (72189-088-03)
71205-503-03 71205-503 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20210226 N/A ANDA ANDA210001 Proficient Rx LP AZITHROMYCIN DIHYDRATE 500 mg/1 1 BLISTER PACK in 1 BAG (71205-503-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK
71335-1755-1 71335-1755 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20211220 N/A ANDA ANDA210001 Bryant Ranch Prepack AZITHROMYCIN DIHYDRATE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1755-1)
71335-1755-2 71335-1755 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20211220 N/A ANDA ANDA210001 Bryant Ranch Prepack AZITHROMYCIN DIHYDRATE 500 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (71335-1755-2)
68071-2297-2 68071-2297 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20201116 N/A ANDA ANDA210001 NuCare Pharmaceuticals,Inc. AZITHROMYCIN DIHYDRATE 500 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (68071-2297-2)
42291-083-03 42291-083 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA210001 AvKARE AZITHROMYCIN DIHYDRATE 500 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (42291-083-03)
42291-083-30 42291-083 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20220411 N/A ANDA ANDA210001 AvKARE AZITHROMYCIN DIHYDRATE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42291-083-30)
70518-3169-1 70518-3169 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20240426 N/A ANDA ANDA210001 REMEDYREPACK INC. AZITHROMYCIN DIHYDRATE 500 mg/1 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3169-1)
70518-3169-2 70518-3169 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA210001 REMEDYREPACK INC. AZITHROMYCIN DIHYDRATE 500 mg/1 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3169-2)
53002-4221-2 53002-4221 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20230831 N/A ANDA ANDA210001 RPK Pharmaceuticals, Inc. AZITHROMYCIN DIHYDRATE 500 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (53002-4221-2)
53002-4221-5 53002-4221 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20230831 N/A ANDA ANDA210001 RPK Pharmaceuticals, Inc. AZITHROMYCIN DIHYDRATE 500 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (53002-4221-5)
53002-4221-6 53002-4221 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20230831 N/A ANDA ANDA210001 RPK Pharmaceuticals, Inc. AZITHROMYCIN DIHYDRATE 500 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (53002-4221-6)
53002-4221-9 53002-4221 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20230831 N/A ANDA ANDA210001 RPK Pharmaceuticals, Inc. AZITHROMYCIN DIHYDRATE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (53002-4221-9)
69452-172-13 69452-172 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20190312 N/A ANDA ANDA210001 Bionpharma Inc. AZITHROMYCIN DIHYDRATE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69452-172-13)
69452-172-72 69452-172 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20191010 N/A ANDA ANDA210001 Bionpharma Inc. AZITHROMYCIN DIHYDRATE 500 mg/1 3 BLISTER PACK in 1 CARTON (69452-172-72) / 3 TABLET, FILM COATED in 1 BLISTER PACK
69452-172-74 69452-172 HUMAN PRESCRIPTION DRUG Azithromycin Azithromycin TABLET, FILM COATED ORAL 20191010 N/A ANDA ANDA210001 Bionpharma Inc. AZITHROMYCIN DIHYDRATE 500 mg/1 1 BLISTER PACK in 1 CARTON (69452-172-74) / 3 TABLET, FILM COATED in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase