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=ANDA075274"
符合检索条件的记录共 43 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
71335-3104-2 71335-3104 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20260316 20271130 ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-3104-2)
71335-3104-3 71335-3104 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20260316 20271130 ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-3104-3)
71335-3104-4 71335-3104 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20260316 20271130 ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71335-3104-4)
71335-3104-5 71335-3104 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20260316 20271130 ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-3104-5)
71335-3104-6 71335-3104 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20260316 20271130 ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-3104-6)
71335-3104-7 71335-3104 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20260316 20271130 ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-3104-7)
71335-3040-1 71335-3040 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20251203 N/A ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-3040-1)
71335-2987-1 71335-2987 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20240215 20280630 ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2987-1)
63629-1047-1 63629-1047 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20130923 20271130 ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63629-1047-1)
53401-008-31 53401-008 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20260414 20280630 ANDA ANDA075274 Aphena Pharma Solutions - Tennessee, LLC NALTREXONE HYDROCHLORIDE 50 mg/1 600 TABLET, FILM COATED in 1 BOTTLE (53401-008-31)
72162-1566-1 72162-1566 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20230912 N/A ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-1566-1)
72162-1566-3 72162-1566 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20230912 N/A ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72162-1566-3)
72162-2529-1 72162-2529 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20250903 N/A ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2529-1)
72162-2529-3 72162-2529 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20250903 N/A ANDA ANDA075274 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72162-2529-3)
64850-300-01 64850-300 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20250815 N/A ANDA ANDA075274 Elite Laboratories, Inc. NALTREXONE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (64850-300-01)
64850-300-30 64850-300 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20250815 N/A ANDA ANDA075274 Elite Laboratories, Inc. NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (64850-300-30)
68094-853-61 68094-853 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride naltrexone Hydrochloride TABLET, FILM COATED ORAL 20240815 N/A ANDA ANDA075274 Precision Dose Inc. NALTREXONE HYDROCHLORIDE 50 mg/1 10 BLISTER PACK in 1 CARTON (68094-853-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)
68094-853-62 68094-853 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride naltrexone Hydrochloride TABLET, FILM COATED ORAL 20141029 20261231 ANDA ANDA075274 Precision Dose Inc. NALTREXONE HYDROCHLORIDE 50 mg/1 3 BLISTER PACK in 1 CARTON (68094-853-62) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)
68094-853-66 68094-853 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride naltrexone Hydrochloride TABLET, FILM COATED ORAL 20240815 N/A ANDA ANDA075274 Precision Dose Inc. NALTREXONE HYDROCHLORIDE 50 mg/1 2 BLISTER PACK in 1 CARTON (68094-853-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)
68071-3654-3 68071-3654 HUMAN PRESCRIPTION DRUG Naltrexone Hydrochloride Naltrexone Hydrochloride TABLET, FILM COATED ORAL 20240724 N/A ANDA ANDA075274 NuCare Pharmaceuticals Inc. NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3654-3)
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