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
71205-155-10 71205-155 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20240514 N/A ANDA ANDA088618 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-155-10)
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)
71335-0935-1 71335-0935 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20180828 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0935-1)
71335-0935-2 71335-0935 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20180828 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0935-2)
71335-0935-3 71335-0935 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20180828 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-0935-3)
71335-0935-4 71335-0935 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20180828 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-0935-4)
71335-0935-5 71335-0935 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20180828 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-0935-5)
71335-0935-6 71335-0935 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20180828 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0935-6)
71335-0935-7 71335-0935 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20180828 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 19 TABLET, FILM COATED in 1 BOTTLE (71335-0935-7)
71335-0935-8 71335-0935 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20180828 N/A ANDA ANDA088618 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-0935-8)
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)
61919-743-15 61919-743 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE HYDROXYZINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20200616 N/A ANDA ANDA088618 DIRECT RX HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (61919-743-15)
61919-743-30 61919-743 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE HYDROXYZINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20200616 N/A ANDA ANDA088618 DIRECT RX HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (61919-743-30)
61919-743-60 61919-743 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE HYDROXYZINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20200616 N/A ANDA ANDA088618 DIRECT RX HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (61919-743-60)
61919-743-90 61919-743 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE HYDROXYZINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20200616 N/A ANDA ANDA088618 DIRECT RX HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (61919-743-90)
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