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=ANDA077712"
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
76420-366-05 76420-366 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20240910 N/A ANDA ANDA077712 Asclemed USA, Inc. OXYCODONE HYDROCHLORIDE 30 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (76420-366-05)
76420-366-30 76420-366 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20250527 N/A ANDA ANDA077712 Asclemed USA, Inc. OXYCODONE HYDROCHLORIDE 30 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (76420-366-30)
76420-366-60 76420-366 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20250527 N/A ANDA ANDA077712 Asclemed USA, Inc. OXYCODONE HYDROCHLORIDE 30 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (76420-366-60)
76420-366-90 76420-366 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20250527 N/A ANDA ANDA077712 Asclemed USA, Inc. OXYCODONE HYDROCHLORIDE 30 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (76420-366-90)
71335-2816-1 71335-2816 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251016 N/A ANDA ANDA077712 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 30 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (71335-2816-1)
71335-2816-2 71335-2816 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251016 N/A ANDA ANDA077712 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 30 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71335-2816-2)
71335-2816-3 71335-2816 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251016 N/A ANDA ANDA077712 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 30 mg/1 120 TABLET in 1 BOTTLE, PLASTIC (71335-2816-3)
71335-2816-4 71335-2816 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251016 N/A ANDA ANDA077712 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 30 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (71335-2816-4)
71335-2816-5 71335-2816 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251016 N/A ANDA ANDA077712 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 30 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (71335-2816-5)
71335-2816-6 71335-2816 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251016 N/A ANDA ANDA077712 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 30 mg/1 40 TABLET in 1 BOTTLE, PLASTIC (71335-2816-6)
71335-2816-7 71335-2816 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251016 N/A ANDA ANDA077712 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 30 mg/1 18 TABLET in 1 BOTTLE, PLASTIC (71335-2816-7)
71335-2816-8 71335-2816 HUMAN PRESCRIPTION DRUG Oxycodone Hydrochloride Oxycodone Hydrochloride TABLET ORAL 20251016 N/A ANDA ANDA077712 Bryant Ranch Prepack OXYCODONE HYDROCHLORIDE 30 mg/1 28 TABLET in 1 BOTTLE, PLASTIC (71335-2816-8)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase