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=ANDA207743"
符合检索条件的记录共 42 条，共 3 页，当前第 2 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
68382-800-16 68382-800 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Pharmaceuticals USA Inc. LABETALOL HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-800-16)
71335-1242-1 71335-1242 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191127 N/A ANDA ANDA207743 Bryant Ranch Prepack LABETALOL HYDROCHLORIDE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1242-1)
71335-1242-2 71335-1242 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20210723 N/A ANDA ANDA207743 Bryant Ranch Prepack LABETALOL HYDROCHLORIDE 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1242-2)
71335-1242-3 71335-1242 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20190606 N/A ANDA ANDA207743 Bryant Ranch Prepack LABETALOL HYDROCHLORIDE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1242-3)
60687-439-01 60687-439 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20190716 N/A ANDA ANDA207743 American Health Packaging LABETALOL HYDROCHLORIDE 100 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-439-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-439-11)
60687-450-01 60687-450 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20190716 N/A ANDA ANDA207743 American Health Packaging LABETALOL HYDROCHLORIDE 200 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-450-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-450-11)
60687-461-01 60687-461 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20190716 N/A ANDA ANDA207743 American Health Packaging LABETALOL HYDROCHLORIDE 300 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-461-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-461-11)
70771-1163-1 70771-1163 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1163-1)
70771-1163-3 70771-1163 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1163-3)
70771-1163-5 70771-1163 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70771-1163-5)
70771-1163-9 70771-1163 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1163-9)
70771-1164-1 70771-1164 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1164-1)
0904-7111-61 0904-7111 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 20241130 ANDA ANDA207743 Major Pharmaceuticals LABETALOL HYDROCHLORIDE 300 mg/1 100 BLISTER PACK in 1 CARTON (0904-7111-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7110-61 0904-7110 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 20241231 ANDA ANDA207743 Major Pharmaceuticals LABETALOL HYDROCHLORIDE 200 mg/1 100 BLISTER PACK in 1 CARTON (0904-7110-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7109-61 0904-7109 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 20241231 ANDA ANDA207743 Major Pharmaceuticals LABETALOL HYDROCHLORIDE 100 mg/1 100 BLISTER PACK in 1 CARTON (0904-7109-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
70771-1164-3 70771-1164 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1164-3)
70771-1164-5 70771-1164 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70771-1164-5)
70771-1164-9 70771-1164 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1164-9)
70771-1165-1 70771-1165 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1165-1)
70771-1165-3 70771-1165 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20171205 N/A ANDA ANDA207743 Zydus Lifesciences Limited LABETALOL HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1165-3)
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