Wednesday, July 22, 2026
News

Alembic Pharma partner NATCO gets USFDA tentative nod for generic Olaparib tablets; US market size at USD 1.4 bn

SocialTwist Tell-a-Friend    Print this Page   COMMENT

New Delhi | July 19, 2026 12:56:21 PM IST
Alembic Pharmaceuticals said its partner NATCO Pharma has received tentative approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Olaparib Tablets in 100 mg and 150 mg strengths, a generic equivalent of AstraZeneca's Lynparza tablets.

The approval is for the indication covered under the approved labelling of the reference listed drug. Alembic Pharmaceuticals will distribute the product in the United States, while NATCO Pharma will manufacture the tablets.

The product is expected to address a significant market opportunity in the US. Olaparib Tablets in the 100 mg and 150 mg strengths had an estimated market size of around USD 1.4 billion for the 12 months ended March 2026, according to IQVIA data cited by the company.

However, the commercial launch timeline remains subject to the ongoing Paragraph IV litigation related to the product. The tentative approval therefore marks a regulatory milestone, while the outcome of the litigation will remain an important factor for the product's market entry.

Olaparib is a PARP inhibitor used in the treatment of certain cancers and is marketed as Lynparza by AstraZeneca. The approval strengthens Alembic's product pipeline in the US generic pharmaceutical market and expands its portfolio of products targeting large-market opportunities.

Alembic Pharmaceuticals' cumulative tally of USFDA ANDA approvals has risen to 244, comprising 224 final approvals and 20 tentative approvals.

Alembic Pharmaceuticals is a vertically integrated research and development-focused pharmaceutical company with operations spanning generic medicines and branded generics. The company manufactures and markets generic pharmaceutical products globally and operates research and manufacturing facilities approved by regulatory authorities in developed markets, including the USFDA.

The latest approval comes as Indian pharmaceutical companies continue to expand their presence in the US generic market through partnerships, complex products and large-market opportunities. For Alembic, the approval provides another potential growth avenue, although the ongoing litigation and the eventual commercial launch remain key monitorables. (ANI)

 
  LATEST COMMENTS ()
POST YOUR COMMENT
Comments Not Available
 
POST YOUR COMMENT
 
 
TRENDING TOPICS
 
 
CITY NEWS
MORE CITIES
 
 
 
MORE BUSINESS NEWS
Istituto Marangoni Mumbai Presents Its 2...
Cement makers' margins to fall Rs 50-75/...
FDA's ruling on Nicotine raises case for...
Draft Telecommunications Rules 2026 aim ...
'A Young Changemaker's Vision' for Emerg...
TRAI expects satellite communication fra...
More...
 
INDIA WORLD ASIA
'Opposition using students as political ...
Govt acting scared, must explain why Dha...
Andhra Pradesh Chief Minister N Chandrab...
Robert Vadra backs students' protests, s...
SC refuses to cancel Chaitanya Baghel's ...
Priyanka Gandhi slams Centre; asks why l...
More...    
 
 Top Stories
Defence Ministry to buy 10 MALE dro... 
Lula signs law to strengthen Brazil... 
BRS leader KTR writes to Telangana ... 
Union Minister Jitendra Singh outli... 
"Mental wellness and healthy lifest... 
US attacks Larak Island in the Stra... 
Delhi Police ACP injured after ston... 
Trump says US will bomb "one bridge...