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=NDA021392"
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
0187-2048-90 0187-2048 HUMAN PRESCRIPTION DRUG Cardizem LA Diltiazem Hydrochloride TABLET, EXTENDED RELEASE ORAL 20101225 N/A NDA NDA021392 Bausch Health US LLC DILTIAZEM HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2048-90)
0187-2049-30 0187-2049 HUMAN PRESCRIPTION DRUG Cardizem LA Diltiazem Hydrochloride TABLET, EXTENDED RELEASE ORAL 20101225 N/A NDA NDA021392 Bausch Health US LLC DILTIAZEM HYDROCHLORIDE 360 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-30)
0187-2049-90 0187-2049 HUMAN PRESCRIPTION DRUG Cardizem LA Diltiazem Hydrochloride TABLET, EXTENDED RELEASE ORAL 20101225 N/A NDA NDA021392 Bausch Health US LLC DILTIAZEM HYDROCHLORIDE 360 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2049-90)
0187-2050-30 0187-2050 HUMAN PRESCRIPTION DRUG Cardizem LA Diltiazem Hydrochloride TABLET, EXTENDED RELEASE ORAL 20101225 N/A NDA NDA021392 Bausch Health US LLC DILTIAZEM HYDROCHLORIDE 420 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2050-30)
0187-2050-90 0187-2050 HUMAN PRESCRIPTION DRUG Cardizem LA Diltiazem Hydrochloride TABLET, EXTENDED RELEASE ORAL 20101225 N/A NDA NDA021392 Bausch Health US LLC DILTIAZEM HYDROCHLORIDE 420 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2050-90)
72162-1902-3 72162-1902 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride Extended-Release Tablets TABLET, EXTENDED RELEASE ORAL 20240321 N/A NDA AUTHORIZED GENERIC NDA021392 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 180 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1902-3)
72162-1903-3 72162-1903 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride Extended-Release Tablets TABLET, EXTENDED RELEASE ORAL 20240321 N/A NDA AUTHORIZED GENERIC NDA021392 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 240 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1903-3)
72162-1905-3 72162-1905 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride Extended-Release Tablets TABLET, EXTENDED RELEASE ORAL 20240321 N/A NDA AUTHORIZED GENERIC NDA021392 Bryant Ranch Prepack DILTIAZEM HYDROCHLORIDE 360 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1905-3)
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