我们重视您的隐私
我们使用 Cookie 分析网站流量并改善您的体验。请参阅我们的隐私政策。
隶属于 Takeda Pharmaceutical Co., Ltd.
相关临床试验
0
0 进行中
药物批准
10
批准总数
监管机构
2
监管机构数
成立时间
N/A
暂无试验阶段数据
暂无试验数据
NMPA
National Medical Products Administration
8
CANADA
Health Canada
• Lupin has received FDA approval for its generic version of Adderall XR, an extended-release capsule used to treat ADHD in adults and children. • The approved Abbreviated New Drug Application (ANDA) includes multiple dosage strengths, ranging from 5 mg to 30 mg. • Lupin's generic equivalent of Adderall XR is poised to enter a market with annual sales of $865 million, based on IQVIA MAT September 2024 data. • The drug will be manufactured in Lupin’s Somerset facility in the United States, ensuring a domestic supply of this critical medication.