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=ANDA076134"
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
59779-528-31 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 3 BLISTER PACK in 1 CARTON (59779-528-31) / 10 TABLET in 1 BLISTER PACK
59779-528-43 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 1 BOTTLE in 1 CARTON (59779-528-43) / 45 TABLET in 1 BOTTLE
59779-528-56 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 1 BLISTER PACK in 1 CARTON (59779-528-56) / 5 TABLET in 1 BLISTER PACK
59779-528-60 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 1 BOTTLE in 1 CARTON (59779-528-60) / 60 TABLET in 1 BOTTLE
59779-528-69 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 1 BLISTER PACK in 1 CARTON (59779-528-69) / 10 TABLET in 1 BLISTER PACK
59779-528-93 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 2 BOTTLE in 1 CARTON (59779-528-93) / 30 TABLET in 1 BOTTLE
59779-528-37 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 2 BOTTLE in 1 CARTON (59779-528-37) / 120 TABLET in 1 BOTTLE
59779-528-38 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 1 BOTTLE in 1 CARTON (59779-528-38) / 365 TABLET in 1 BOTTLE
59779-528-21 59779-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20100108 N/A ANDA ANDA076134 CVS Pharmacy LORATADINE 10 mg/1 2 BLISTER PACK in 1 CARTON (59779-528-21) / 10 TABLET in 1 BLISTER PACK
53943-975-30 53943-975 HUMAN OTC DRUG Loratadine Allergy Relief Loratadine TABLET ORAL 20171101 N/A ANDA ANDA076134 DISCOUNT DRUG MART LORATADINE 10 mg/1 30 TABLET in 1 BLISTER PACK (53943-975-30)
53943-975-60 53943-975 HUMAN OTC DRUG Loratadine Allergy Relief Loratadine TABLET ORAL 20171101 N/A ANDA ANDA076134 DISCOUNT DRUG MART LORATADINE 10 mg/1 60 TABLET in 1 BOTTLE (53943-975-60)
63868-151-30 63868-151 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20030819 N/A ANDA ANDA076134 Chain Drug Marketing Association Inc. LORATADINE 10 mg/1 30 TABLET in 1 BLISTER PACK (63868-151-30)
63868-151-01 63868-151 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20030819 N/A ANDA ANDA076134 Chain Drug Marketing Association Inc. LORATADINE 10 mg/1 100 TABLET in 1 BOTTLE (63868-151-01)
63868-151-10 63868-151 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20030819 N/A ANDA ANDA076134 Chain Drug Marketing Association Inc. LORATADINE 10 mg/1 10 TABLET in 1 BLISTER PACK (63868-151-10)
67091-246-30 67091-246 HUMAN OTC DRUG Loratadine Allergy Relief Loratadine TABLET ORAL 20150108 N/A ANDA ANDA076134 WinCo Foods, LLC LORATADINE 10 mg/1 30 BLISTER PACK in 1 CARTON (67091-246-30) / 1 TABLET in 1 BLISTER PACK
55315-528-69 55315-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20030819 N/A ANDA ANDA076134 Fred's Inc. LORATADINE 10 mg/1 10 TABLET in 1 BLISTER PACK (55315-528-69)
55315-528-31 55315-528 HUMAN OTC DRUG Loratadine Loratadine TABLET ORAL 20030819 N/A ANDA ANDA076134 Fred's Inc. LORATADINE 10 mg/1 30 TABLET in 1 BLISTER PACK (55315-528-31)
67091-245-10 67091-245 HUMAN OTC DRUG Loratadine Allergy Relief Loratadine TABLET ORAL 20150108 N/A ANDA ANDA076134 WinCo Foods, LLC LORATADINE 10 mg/1 10 BLISTER PACK in 1 CARTON (67091-245-10) / 1 TABLET in 1 BLISTER PACK
50090-2387-0 50090-2387 HUMAN OTC DRUG Loratadine Allergy Relief Loratadine TABLET ORAL 20171101 N/A ANDA ANDA076134 A-S Medication Solutions LORATADINE 10 mg/1 30 TABLET in 1 BLISTER PACK (50090-2387-0)
82652-021-01 82652-021 HUMAN OTC DRUG Diphen Benzocaine, Benzalkonium chloride, Lidocaine hydrochloride, Hydrocortisone, Bacitracin zinc, Neomycin sulfate, Polymyxin B sulfate, Calcium Carbonate, Ibuprofen, Loratadine, Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, Diphenhydramine Hydrochloride, Potassium Chloride, Magnesium Oxide, Meclizine Hydrochloride, and Bismuth Subsalicylate KIT 20220510 N/A ANDA ANDA076134 Remedy Pack LLC 1 KIT in 1 CARTON (82652-021-01) * 1 TABLET, FILM COATED in 1 PACKET (82652-022-01) * 2 TABLET, FILM COATED in 1 PACKET (82652-025-01) * 2 TABLET in 1 PACKET (82652-030-01) * 2 TABLET in 1 PACKET * 1 TABLET, FILM COATED in 1 PACKET (82652-031-01) * 2 TABLET in 1 PACKET (82652-032-01) * 2 TABLET, CHEWABLE in 1 PACKET (82652-026-01) * 2 TABLET, FILM COATED in 1 PACKET (82652-024-01) * 2 TABLET, CHEWABLE in 1 PACKET (82652-023-01) * .5 g in 1 PACKET (82652-028-01) * .9 g in 1 PACKET (82652-027-01) * .9 g in 1 PACKET (82652-029-01) * .75 g in 1 PACKET (82652-033-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase