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=ANDA074910"
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
51079-926-20 51079-926 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 19991215 N/A ANDA ANDA074910 Mylan Institutional Inc. DILTIAZEM HYDROCHLORIDE 120 mg/1 100 BLISTER PACK in 1 CARTON (51079-926-20) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-926-01)
51079-925-20 51079-925 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 19991215 N/A ANDA ANDA074910 Mylan Institutional Inc. DILTIAZEM HYDROCHLORIDE 90 mg/1 100 BLISTER PACK in 1 CARTON (51079-925-20) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-925-01)
51079-924-20 51079-924 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 19991215 N/A ANDA ANDA074910 Mylan Institutional Inc. DILTIAZEM HYDROCHLORIDE 60 mg/1 100 BLISTER PACK in 1 CARTON (51079-924-20) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-924-01)
0378-6060-01 0378-6060 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 19970502 N/A ANDA ANDA074910 Mylan Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 60 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6060-01)
0378-6090-01 0378-6090 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 19970502 N/A ANDA ANDA074910 Mylan Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 90 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6090-01)
0378-6120-01 0378-6120 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 19970502 N/A ANDA ANDA074910 Mylan Pharmaceuticals Inc. DILTIAZEM HYDROCHLORIDE 120 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6120-01)
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