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=ANDA074185"
符合检索条件的记录共 19 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0615-8032-39 0615-8032 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20160510 N/A ANDA ANDA074185 NCS HealthCare of KY, LLC dba Vangard Labs DILTIAZEM HYDROCHLORIDE 30 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8032-39)
0093-0319-05 0093-0319 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 19951230 N/A ANDA ANDA074185 Teva Pharmaceuticals USA, Inc. DILTIAZEM HYDROCHLORIDE 60 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (0093-0319-05)
0093-0319-01 0093-0319 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 19951222 N/A ANDA ANDA074185 Teva Pharmaceuticals USA, Inc. DILTIAZEM HYDROCHLORIDE 60 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0093-0319-01)
51655-020-52 51655-020 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20220811 N/A ANDA ANDA074185 Northwind Pharmaceuticals, LLC DILTIAZEM HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-020-52)
60687-728-01 60687-728 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20231201 N/A ANDA ANDA074185 American Health Packaging DILTIAZEM HYDROCHLORIDE 60 mg/1 100 BLISTER PACK in 1 CARTON (60687-728-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-728-11)
0093-0318-01 0093-0318 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 19951222 N/A ANDA ANDA074185 Teva Pharmaceuticals USA, Inc. DILTIAZEM HYDROCHLORIDE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0093-0318-01)
0093-0318-05 0093-0318 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 19951228 N/A ANDA ANDA074185 Teva Pharmaceuticals USA, Inc. DILTIAZEM HYDROCHLORIDE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (0093-0318-05)
63187-769-10 63187-769 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20161101 N/A ANDA ANDA074185 Proficient Rx LP DILTIAZEM HYDROCHLORIDE 120 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (63187-769-10)
63187-769-30 63187-769 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20161101 N/A ANDA ANDA074185 Proficient Rx LP DILTIAZEM HYDROCHLORIDE 120 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-769-30)
63187-769-60 63187-769 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20161101 N/A ANDA ANDA074185 Proficient Rx LP DILTIAZEM HYDROCHLORIDE 120 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-769-60)
63187-769-90 63187-769 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20230524 N/A ANDA ANDA074185 Proficient Rx LP DILTIAZEM HYDROCHLORIDE 120 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-769-90)
60687-717-01 60687-717 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20230327 N/A ANDA ANDA074185 American Health Packaging DILTIAZEM HYDROCHLORIDE 30 mg/1 100 BLISTER PACK in 1 CARTON (60687-717-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-717-11)
0093-0321-01 0093-0321 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 19951226 N/A ANDA ANDA074185 Teva Pharmaceuticals USA, Inc. DILTIAZEM HYDROCHLORIDE 120 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0093-0321-01)
63629-3659-1 63629-3659 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20240327 N/A ANDA ANDA074185 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63629-3659-1)
0615-8033-39 0615-8033 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20160517 N/A ANDA ANDA074185 NCS HealthCare of KY, LLC dba Vangard Labs DILTIAZEM HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8033-39)
0093-0320-01 0093-0320 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 19951222 N/A ANDA ANDA074185 Teva Pharmaceuticals USA, Inc. DILTIAZEM HYDROCHLORIDE 90 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0093-0320-01)
50090-0451-0 50090-0451 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20181025 N/A ANDA ANDA074185 A-S Medication Solutions DILTIAZEM HYDROCHLORIDE 60 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-0451-0)
50090-0451-2 50090-0451 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20160629 N/A ANDA ANDA074185 A-S Medication Solutions DILTIAZEM HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-0451-2)
50090-0451-3 50090-0451 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20180516 N/A ANDA ANDA074185 A-S Medication Solutions DILTIAZEM HYDROCHLORIDE 60 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-0451-3)
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