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=ANDA218032"
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
50742-566-01 50742-566 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250703 N/A ANDA ANDA218032 Ingenus Pharmaceuticals, LLC DILTIAZEM HYDROCHLORIDE 120 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-566-01)
50742-566-05 50742-566 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250703 N/A ANDA ANDA218032 Ingenus Pharmaceuticals, LLC DILTIAZEM HYDROCHLORIDE 120 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-566-05)
50742-565-01 50742-565 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250703 N/A ANDA ANDA218032 Ingenus Pharmaceuticals, LLC DILTIAZEM HYDROCHLORIDE 90 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-565-01)
50742-565-05 50742-565 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250703 N/A ANDA ANDA218032 Ingenus Pharmaceuticals, LLC DILTIAZEM HYDROCHLORIDE 90 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-565-05)
50742-564-01 50742-564 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250703 N/A ANDA ANDA218032 Ingenus Pharmaceuticals, LLC DILTIAZEM HYDROCHLORIDE 60 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-564-01)
50742-564-05 50742-564 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20250703 N/A ANDA ANDA218032 Ingenus Pharmaceuticals, LLC DILTIAZEM HYDROCHLORIDE 60 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-564-05)
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