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"
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
10135-712-05 10135-712 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol TABLET, FILM COATED ORAL 20201001 N/A ANDA ANDA075215 Marlex Pharmaceuticals Inc LABETALOL 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (10135-712-05)
10135-712-01 10135-712 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol TABLET, FILM COATED ORAL 20201001 N/A ANDA ANDA075215 Marlex Pharmaceuticals Inc LABETALOL 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (10135-712-01)
10135-711-05 10135-711 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol TABLET, FILM COATED ORAL 20201001 N/A ANDA ANDA075215 Marlex Pharmaceuticals Inc LABETALOL 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (10135-711-05)
10135-711-01 10135-711 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol TABLET, FILM COATED ORAL 20201001 N/A ANDA ANDA075215 Marlex Pharmaceuticals Inc LABETALOL 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (10135-711-01)
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)
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)
63629-1161-1 63629-1161 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 (63629-1161-1)
63629-1166-1 63629-1166 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (63629-1166-1)
63629-1162-1 63629-1162 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 (63629-1162-1)
63629-1165-1 63629-1165 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63629-1165-1)
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)
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)
71335-9690-5 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)
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)
71335-9690-1 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 30 TABLET, FILM COATED in 1 BOTTLE (71335-9690-1)
71335-9690-2 71335-9690 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20230321 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 300 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-9690-2)
58657-602-01 58657-602 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Method Pharmaceuticals, LLC LABETALOL 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (58657-602-01)
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)
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