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=ANDA088618"
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
72789-216-30 72789-216 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20211130 N/A ANDA ANDA088618 PD-Rx Pharmaceuticals, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-30)
72789-216-40 72789-216 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20211118 N/A ANDA ANDA088618 PD-Rx Pharmaceuticals, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-40)
72789-216-60 72789-216 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20220624 N/A ANDA ANDA088618 PD-Rx Pharmaceuticals, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-60)
72789-216-90 72789-216 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20211208 N/A ANDA ANDA088618 PD-Rx Pharmaceuticals, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-90)
51655-589-52 51655-589 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20230627 N/A ANDA ANDA088618 Northwind Pharmaceuticals, LLC HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-52)
51655-589-53 51655-589 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA088618 Northwind Pharmaceuticals, LLC HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-53)
63629-8740-1 63629-8740 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20210827 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63629-8740-1)
70518-2279-0 70518-2279 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20190824 N/A ANDA ANDA088618 REMEDYREPACK INC. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2279-0)
0093-5061-01 0093-5061 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20121009 N/A ANDA ANDA088618 Teva Pharmaceuticals USA, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0093-5061-01)
0093-5061-05 0093-5061 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20121010 N/A ANDA ANDA088618 Teva Pharmaceuticals USA, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (0093-5061-05)
0093-5061-10 0093-5061 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20121011 N/A ANDA ANDA088618 Teva Pharmaceuticals USA, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0093-5061-10)
55154-2148-0 55154-2148 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20251022 N/A ANDA ANDA088618 Cardinal Health 107, LLC HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 10 BLISTER PACK in 1 BAG (55154-2148-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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