Dr. Reddy';s Laboratories Announces the Launch of Pemetrexed for Injection USP, in the U.S. Market
Dr. Reddy's Laboratories Ltd. has launched Pemetrexed for Injection in 100 mg and 500 mg single-dose vials, approved by the USFDA. This generic version is an equivalent to ALIMTA®, which generated approximately $1.24 billion in US sales for the twelve months ending March 2022. The introduction of this generic product expands Dr. Reddy's offerings in oncology and positions the company in a significant market segment, potentially benefiting its financial growth.
- Launch of Pemetrexed for Injection enhances product portfolio in oncology.
- Approval by USFDA positions Dr. Reddy's favorably in the competitive generics market.
- Access to a market with approximately $1.24 billion in annual sales increases revenue potential.
- None.
The ALIMTA® brand and generic had
Dr. Reddy’s Pemetrexed for Injection is supplied in 100 mg and 500 mg single-dose vials.
Click here for full prescribing information.
ALIMTA is a trademark of Eli Lilly and Company
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RDY-0522-413
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Source: Dr. Reddy’s
FAQ
What is the significance of Dr. Reddy's new Pemetrexed product launch?
When was Pemetrexed for Injection approved by the USFDA?
What are the available dosages for Dr. Reddy's Pemetrexed for Injection?
How does Pemetrexed for Injection compare to ALIMTA® in terms of market potential?