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=ANDA076588"
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
63304-905-03 63304-905 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 1 g/1 10 TABLET, FILM COATED in 1 BOTTLE (63304-905-03)
63304-905-05 63304-905 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 1 g/1 500 TABLET, FILM COATED in 1 BOTTLE (63304-905-05)
63304-905-30 63304-905 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 1 g/1 30 TABLET, FILM COATED in 1 BOTTLE (63304-905-30)
63304-905-77 63304-905 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 1 g/1 100 BLISTER PACK in 1 CARTON (63304-905-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (63304-905-11)
63304-905-90 63304-905 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 1 g/1 90 TABLET, FILM COATED in 1 BOTTLE (63304-905-90)
63304-904-03 63304-904 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (63304-904-03)
63304-904-05 63304-904 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (63304-904-05)
63304-904-30 63304-904 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63304-904-30)
63304-904-77 63304-904 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 100 BLISTER PACK in 1 CARTON (63304-904-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (63304-904-11)
63304-904-90 63304-904 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20201219 N/A ANDA ANDA076588 SUN PHARMACEUTICAL INDUSTRIES, INC. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63304-904-90)
51407-108-30 51407-108 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20220627 N/A ANDA ANDA076588 Golden State Medical Supply, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 30 TABLET, FILM COATED in 1 BOTTLE (51407-108-30)
51407-108-90 51407-108 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20220627 N/A ANDA ANDA076588 Golden State Medical Supply, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 90 TABLET, FILM COATED in 1 BOTTLE (51407-108-90)
51407-107-30 51407-107 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20220627 N/A ANDA ANDA076588 Golden State Medical Supply, Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (51407-107-30)
51407-107-90 51407-107 HUMAN PRESCRIPTION DRUG Valacyclovir Valacyclovir TABLET, FILM COATED ORAL 20220627 N/A ANDA ANDA076588 Golden State Medical Supply, Inc. VALACYCLOVIR HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (51407-107-90)
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