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=ANDA075215"
符合检索条件的记录共 45 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
71335-9690-3 71335-9690 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 300 mg/1 58 TABLET, FILM COATED in 1 BOTTLE (71335-9690-3)
71335-9690-4 71335-9690 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-9690-4)
71335-9690-5 71335-9690 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 300 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-9690-5)
71247-127-01 71247-127 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA075215 Innogenix, Inc. LABETALOL HYDROCHLORIDE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71247-127-01)
71247-127-05 71247-127 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA075215 Innogenix, Inc. LABETALOL HYDROCHLORIDE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (71247-127-05)
50090-6833-1 50090-6833 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20231121 N/A ANDA ANDA075215 A-S Medication Solutions LABETALOL HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6833-1)
63629-1164-1 63629-1164 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20201002 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (63629-1164-1)
72162-1675-1 72162-1675 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-1675-1)
72162-1675-5 72162-1675 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-1675-5)
58657-604-01 58657-604 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Method Pharmaceuticals, LLC LABETALOL 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (58657-604-01)
58657-604-50 58657-604 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Method Pharmaceuticals, LLC LABETALOL 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (58657-604-50)
10135-713-01 10135-713 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol TABLET, FILM COATED ORAL 20201001 N/A ANDA ANDA075215 Marlex Pharmaceuticals Inc LABETALOL 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (10135-713-01)
10135-713-05 10135-713 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol TABLET, FILM COATED ORAL 20201001 N/A ANDA ANDA075215 Marlex Pharmaceuticals Inc LABETALOL 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (10135-713-05)
58657-907-01 58657-907 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA075215 Method Pharmaceuticals, LLC LABETALOL 200 mg/1 100 BLISTER PACK in 1 CARTON (58657-907-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (58657-907-10)
71247-126-01 71247-126 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA075215 Innogenix, Inc. LABETALOL HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71247-126-01)
71247-126-05 71247-126 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA075215 Innogenix, Inc. LABETALOL HYDROCHLORIDE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (71247-126-05)
63629-1163-1 63629-1163 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63629-1163-1)
71335-2057-1 71335-2057 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2057-1)
71335-2057-2 71335-2057 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2057-2)
71335-2057-3 71335-2057 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20220303 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2057-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase