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
71205-155-16 71205-155 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA088618 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 16 TABLET, FILM COATED in 1 BOTTLE (71205-155-16)
71205-155-20 71205-155 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA088618 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-155-20)
71205-155-30 71205-155 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA088618 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-155-30)
71205-155-60 71205-155 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA088618 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-155-60)
60760-971-30 60760-971 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20240409 N/A ANDA ANDA088618 ST. MARY'S MEDICAL PARK PHARMACY HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-971-30)
72789-216-04 72789-216 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20230817 N/A ANDA ANDA088618 PD-Rx Pharmaceuticals, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-04)
72789-216-12 72789-216 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20220214 N/A ANDA ANDA088618 PD-Rx Pharmaceuticals, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-12)
72789-216-20 72789-216 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20220324 N/A ANDA ANDA088618 PD-Rx Pharmaceuticals, Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-216-20)
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)
60687-675-01 60687-675 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20221020 N/A ANDA ANDA088618 American Health Packaging HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 100 BLISTER PACK in 1 CARTON (60687-675-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-675-11)
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)
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