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=ANDA217633"
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
62332-782-31 62332-782 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 60 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62332-782-31)
62332-782-71 62332-782 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 60 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62332-782-71)
46708-784-31 46708-784 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Limited DILTIAZEM HYDROCHLORIDE 120 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-784-31)
46708-784-71 46708-784 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Limited DILTIAZEM HYDROCHLORIDE 120 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (46708-784-71)
62332-781-31 62332-781 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62332-781-31)
62332-781-71 62332-781 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62332-781-71)
46708-781-31 46708-781 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Limited DILTIAZEM HYDROCHLORIDE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-781-31)
46708-781-71 46708-781 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Limited DILTIAZEM HYDROCHLORIDE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (46708-781-71)
46708-783-31 46708-783 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Limited DILTIAZEM HYDROCHLORIDE 90 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-783-31)
46708-783-71 46708-783 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Limited DILTIAZEM HYDROCHLORIDE 90 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (46708-783-71)
62332-784-31 62332-784 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 120 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62332-784-31)
62332-784-71 62332-784 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 120 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62332-784-71)
46708-782-31 46708-782 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Limited DILTIAZEM HYDROCHLORIDE 60 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-782-31)
46708-782-71 46708-782 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Limited DILTIAZEM HYDROCHLORIDE 60 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (46708-782-71)
62332-783-31 62332-783 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 90 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62332-783-31)
62332-783-71 62332-783 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride Diltiazem Hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA217633 Alembic Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 90 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62332-783-71)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase