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=NDA018602"
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
70934-854-30 70934-854 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20210423 20250531 NDA AUTHORIZED GENERIC NDA018602 Denton Pharma, Inc. DBA Northwind Pharmaceuticals DILTIAZEM HYDROCHLORIDE 60 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70934-854-30)
0187-0771-47 0187-0771 HUMAN PRESCRIPTION DRUG Cardizem Diltiazem Hydrochloride TABLET, COATED ORAL 20101225 N/A NDA NDA018602 Bausch Health US LLC DILTIAZEM HYDROCHLORIDE 30 mg/1 100 TABLET, COATED in 1 BOTTLE (0187-0771-47)
0187-0772-47 0187-0772 HUMAN PRESCRIPTION DRUG Cardizem Diltiazem Hydrochloride TABLET, COATED ORAL 20101225 N/A NDA NDA018602 Bausch Health US LLC DILTIAZEM HYDROCHLORIDE 60 mg/1 100 TABLET, COATED in 1 BOTTLE (0187-0772-47)
0187-0792-47 0187-0792 HUMAN PRESCRIPTION DRUG Cardizem Diltiazem Hydrochloride TABLET, COATED ORAL 20101225 N/A NDA NDA018602 Bausch Health US LLC DILTIAZEM HYDROCHLORIDE 120 mg/1 100 TABLET, COATED in 1 BOTTLE (0187-0792-47)
63629-9099-1 63629-9099 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20230216 N/A NDA AUTHORIZED GENERIC NDA018602 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 120 mg/1 100 TABLET in 1 BOTTLE (63629-9099-1)
63629-9102-1 63629-9102 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20230216 N/A NDA AUTHORIZED GENERIC NDA018602 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 60 mg/1 100 TABLET in 1 BOTTLE (63629-9102-1)
63629-9104-1 63629-9104 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20230216 N/A NDA AUTHORIZED GENERIC NDA018602 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 90 mg/1 100 TABLET in 1 BOTTLE (63629-9104-1)
68682-006-10 68682-006 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem hydrochloride TABLET ORAL 20101225 N/A NDA AUTHORIZED GENERIC NDA018602 Oceanside Pharmaceuticals DILTIAZEM HYDROCHLORIDE 30 mg/1 100 TABLET in 1 BOTTLE (68682-006-10)
68682-006-50 68682-006 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem hydrochloride TABLET ORAL 20101225 N/A NDA AUTHORIZED GENERIC NDA018602 Oceanside Pharmaceuticals DILTIAZEM HYDROCHLORIDE 30 mg/1 500 TABLET in 1 BOTTLE (68682-006-50)
68682-007-10 68682-007 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20101225 N/A NDA AUTHORIZED GENERIC NDA018602 Oceanside Pharmaceuticals DILTIAZEM HYDROCHLORIDE 60 mg/1 100 TABLET in 1 BOTTLE (68682-007-10)
68682-007-50 68682-007 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20101225 N/A NDA AUTHORIZED GENERIC NDA018602 Oceanside Pharmaceuticals DILTIAZEM HYDROCHLORIDE 60 mg/1 500 TABLET in 1 BOTTLE (68682-007-50)
68682-008-10 68682-008 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20101225 N/A NDA AUTHORIZED GENERIC NDA018602 Oceanside Pharmaceuticals DILTIAZEM HYDROCHLORIDE 90 mg/1 100 TABLET in 1 BOTTLE (68682-008-10)
68682-008-50 68682-008 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20101225 N/A NDA AUTHORIZED GENERIC NDA018602 Oceanside Pharmaceuticals DILTIAZEM HYDROCHLORIDE 90 mg/1 500 TABLET in 1 BOTTLE (68682-008-50)
68682-009-10 68682-009 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20101225 N/A NDA AUTHORIZED GENERIC NDA018602 Oceanside Pharmaceuticals DILTIAZEM HYDROCHLORIDE 120 mg/1 100 TABLET in 1 BOTTLE (68682-009-10)
68071-4242-3 68071-4242 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20180122 N/A NDA AUTHORIZED GENERIC NDA018602 NuCare Pharmaceuticals,Inc. DILTIAZEM HYDROCHLORIDE 120 mg/1 30 TABLET in 1 BOTTLE (68071-4242-3)
71335-0579-1 71335-0579 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20211227 N/A NDA AUTHORIZED GENERIC NDA018602 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 90 mg/1 30 TABLET in 1 BOTTLE (71335-0579-1)
71335-0579-2 71335-0579 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET ORAL 20180313 N/A NDA AUTHORIZED GENERIC NDA018602 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 90 mg/1 90 TABLET in 1 BOTTLE (71335-0579-2)
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