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
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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
72162-1677-1 72162-1677 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 (72162-1677-1)
72162-1677-5 72162-1677 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 (72162-1677-5)
58657-906-01 58657-906 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA075215 Method Pharmaceuticals, LLC LABETALOL 100 mg/1 100 BLISTER PACK in 1 CARTON (58657-906-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58657-906-10)
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)
58657-908-01 58657-908 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA075215 Method Pharmaceuticals, LLC LABETALOL 300 mg/1 100 BLISTER PACK in 1 CARTON (58657-908-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58657-908-10)
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)
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)
10135-711-05 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)
10135-712-01 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)
10135-712-05 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)
10135-713-01 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)
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)
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)
71247-130-01 71247-130 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA075215 Innogenix, Inc. LABETALOL HYDROCHLORIDE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71247-130-01)
71247-130-05 71247-130 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA075215 Innogenix, Inc. LABETALOL HYDROCHLORIDE 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (71247-130-05)
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)
71335-2923-1 71335-2923 HUMAN PRESCRIPTION DRUG Labetalol Hydrochloride Labetalol Hydrochloride TABLET, FILM COATED ORAL 20251029 N/A ANDA ANDA075215 Bryant Ranch Prepack LABETALOL 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (71335-2923-1)
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