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=ANDA200268"
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
65862-512-10 65862-512 HUMAN PRESCRIPTION DRUG PIOGLITAZONE HYDROCHLORIDE pioglitazone hydrochloride TABLET ORAL 20130213 N/A ANDA ANDA200268 Aurobindo Pharma Limited PIOGLITAZONE HYDROCHLORIDE 15 mg/1 3 BLISTER PACK in 1 CARTON (65862-512-10) / 10 TABLET in 1 BLISTER PACK
0904-7090-61 0904-7090 HUMAN PRESCRIPTION DRUG Pioglitazone Pioglitazone TABLET ORAL 20130213 N/A ANDA ANDA200268 Major Pharmaceuticals PIOGLITAZONE HYDROCHLORIDE 15 mg/1 100 BLISTER PACK in 1 CARTON (0904-7090-61) / 1 TABLET in 1 BLISTER PACK
68071-5210-1 68071-5210 HUMAN PRESCRIPTION DRUG Pioglitazone Pioglitazone TABLET ORAL 20200317 N/A ANDA ANDA200268 NuCare Pharmaceuticals,Inc. PIOGLITAZONE HYDROCHLORIDE 30 mg/1 120 TABLET in 1 BOTTLE (68071-5210-1)
50090-7846-0 50090-7846 HUMAN PRESCRIPTION DRUG PIOGLITAZONE HYDROCHLORIDE pioglitazone hydrochloride TABLET ORAL 20251230 N/A ANDA ANDA200268 A-S Medication Solutions PIOGLITAZONE HYDROCHLORIDE 30 mg/1 90 TABLET in 1 BOTTLE (50090-7846-0)
68071-4964-3 68071-4964 HUMAN PRESCRIPTION DRUG Pioglitazone Pioglitazone TABLET ORAL 20190710 N/A ANDA ANDA200268 NuCare Pharmaceuticals,Inc. PIOGLITAZONE HYDROCHLORIDE 30 mg/1 30 TABLET in 1 BOTTLE (68071-4964-3)
70518-4519-0 70518-4519 HUMAN PRESCRIPTION DRUG PIOGLITAZONE HYDROCHLORIDE pioglitazone hydrochloride TABLET ORAL 20251114 N/A ANDA ANDA200268 REMEDYREPACK INC. PIOGLITAZONE HYDROCHLORIDE 45 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-4519-0)
82804-111-30 82804-111 HUMAN PRESCRIPTION DRUG Pioglitazone Pioglitazone TABLET ORAL 20240620 N/A ANDA ANDA200268 Proficient Rx LP PIOGLITAZONE HYDROCHLORIDE 30 mg/1 30 TABLET in 1 BOTTLE (82804-111-30)
68071-5199-3 68071-5199 HUMAN PRESCRIPTION DRUG Pioglitazone Pioglitazone TABLET ORAL 20200310 N/A ANDA ANDA200268 NuCare Pharmaceuticals,Inc. PIOGLITAZONE HYDROCHLORIDE 15 mg/1 30 TABLET in 1 BOTTLE (68071-5199-3)
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