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 50 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
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)
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)
63629-1166-1 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)
72162-1676-1 72162-1676 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 (72162-1676-1)
72162-1676-5 72162-1676 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-1676-5)
71335-2876-1 71335-2876 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20251029 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2876-1)
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)
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)
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)
70518-4201-0 70518-4201 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20241002 N/A ANDA ANDA075215 REMEDYREPACK INC. LABETALOL 100 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4201-0)
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)
58657-602-50 58657-602 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20191122 N/A ANDA ANDA075215 Method Pharmaceuticals, LLC LABETALOL 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (58657-602-50)
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)
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)
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)
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