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AUROBINDO PHARMA LIMITED

🇪🇹Ethiopia
Ownership
-
Employees
-
Market Cap
-
Website

Clinical Trials

13

Active:0
Completed:10

Trial Phases

2 Phases

Phase 3:9
Not Applicable:2

Drug Approvals

446

FDA:363
PPB:37
NMPA:20
+3 more agencies

Drug Approvals

Tadalafil Tablets

Product Name
他达拉非片
Approval Number
国药准字HJ20240105
Approval Date
Oct 9, 2024
NMPA

Tadalafil Tablets

Product Name
他达拉非片
Approval Number
国药准字HJ20240103
Approval Date
Oct 9, 2024
NMPA

Tadalafil Tablets

Product Name
他达拉非片
Approval Number
国药准字HJ20240104
Approval Date
Oct 9, 2024
NMPA

Sertraline Hydrochloride Tablets

Product Name
盐酸舍曲林片
Approval Number
国药准字HJ20230148
Approval Date
Dec 29, 2023
NMPA

Sevelamer Carbonate Tablets

Product Name
碳酸司维拉姆片
Approval Number
国药准字HJ20230122
Approval Date
Dec 29, 2023
NMPA

Fampridine Sustained-release Tablets

Product Name
氨吡啶缓释片
Approval Number
国药准字HJ20230141
Approval Date
Dec 5, 2023
NMPA

Valganciclovir Hydrochloride Tablets

Product Name
盐酸缬更昔洛韦片
Approval Number
国药准字HJ20230121
Approval Date
Oct 24, 2023
NMPA

Olmesartan Medoxomil and Amlodipine Besylate Tablets

Product Name
奥美沙坦酯氨氯地平片
Approval Number
国药准字HJ20230099
Approval Date
Aug 8, 2023
NMPA

Olmesartan Medoxomil and Amlodipine Besylate Tablets

Product Name
奥美沙坦酯氨氯地平片
Approval Number
国药准字HJ20230100
Approval Date
Aug 8, 2023
NMPA

Olmesartan Medoxomil and Amlodipine Besylate Tablets

Product Name
奥美沙坦酯氨氯地平片
Approval Number
国药准字HJ20230101
Approval Date
Aug 8, 2023
NMPA
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Clinical Trials

Distribution across different clinical trial phases (11 trials with phase data)• Click on a phase to view related trials

Phase 3
9 (81.8%)
Not Applicable
2 (18.2%)
No trials found

News

ViiV Healthcare Expands Generic License for Long-Acting HIV Treatment to 133 Countries

ViiV Healthcare has expanded its voluntary licensing agreement with the Medicines Patent Pool to allow generic production of cabotegravir for HIV treatment in 133 countries, including all low-income and Sub-Saharan African nations.

Aurobindo Pharma Secures Multiple FDA Approvals for Generic Drug Portfolio Expansion

Aurobindo Pharma Limited has received FDA approval for multiple generic drug formulations, including critical medications for cardiovascular, neurological, and gastrointestinal conditions.

Aurobindo Receives FDA Approval for Generic Cephalexin Tablets

Aurobindo Pharma has received FDA approval for its generic version of Eli Lilly's Keflet tablets, containing cephalexin in 250 mg and 500 mg dosages.

Generic Manufacturers Secure Licenses for Long-Acting HIV Prevention Drug Cabotegravir

The Medicines Patent Pool has signed sublicense agreements with Aurobindo, Cipla, and Viatris to manufacture generic versions of cabotegravir long-acting for HIV pre-exposure prophylaxis in 90 countries.

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