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=ANDA213324"
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
50090-5772-0 50090-5772 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20211006 N/A ANDA ANDA213324 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (50090-5772-0)
60760-780-30 60760-780 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240508 N/A ANDA ANDA213324 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-780-30)
60760-780-60 60760-780 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240508 N/A ANDA ANDA213324 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-780-60)
60760-780-90 60760-780 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240409 N/A ANDA ANDA213324 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-780-90)
60760-780-92 60760-780 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240416 N/A ANDA ANDA213324 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-780-92)
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