Jump to content
RemedySpot.com

Zydus Cadila receives tentative US FDA approval for Ribavirin tablets

Rate this topic


Guest guest

Recommended Posts

Zydus Cadila receives tentative US FDA approval for Ribavirin tablets

Our Corporate Bureau

3 October 2005

Ahmedabad: Zydus Cadila has received tentative approval from the US FDA for

its abbreviated new drug application (ANDA) for Ribavirin tablets, 200mg.

This anti-viral therapy falls in the anti-infectives segment and will go off

patent in December 2005. The current sales of Ribavirin tablets (200 mg) in

the US market as per NDC Health is estimated at $220 million USD.

The tentative approval for Ribavirin Tablets is the latest in a series of

developments that mark Zydus Cadila's entry in the US generic markets. So

far the group has received seven ANDA approvals. The group recently launched

Atenolol in the US market through its US subsidiary Zydus Pharmaceuticals

USA Inc.

The process of filing ANDAs began in 2003-04 with the group filing 12 ANDAs,

the largest number filed by an Indian company in the very first year of

filing. Till date, the group has filed 27 ANDAs and 32 DMFs.

http://www.domain-b.com/companies/companies_z/zydus/20051003_tentative.html

Link to comment
Share on other sites

Zydus Cadila receives tentative US FDA approval for Ribavirin tablets

Our Corporate Bureau

3 October 2005

Ahmedabad: Zydus Cadila has received tentative approval from the US FDA for

its abbreviated new drug application (ANDA) for Ribavirin tablets, 200mg.

This anti-viral therapy falls in the anti-infectives segment and will go off

patent in December 2005. The current sales of Ribavirin tablets (200 mg) in

the US market as per NDC Health is estimated at $220 million USD.

The tentative approval for Ribavirin Tablets is the latest in a series of

developments that mark Zydus Cadila's entry in the US generic markets. So

far the group has received seven ANDA approvals. The group recently launched

Atenolol in the US market through its US subsidiary Zydus Pharmaceuticals

USA Inc.

The process of filing ANDAs began in 2003-04 with the group filing 12 ANDAs,

the largest number filed by an Indian company in the very first year of

filing. Till date, the group has filed 27 ANDAs and 32 DMFs.

http://www.domain-b.com/companies/companies_z/zydus/20051003_tentative.html

Link to comment
Share on other sites

Zydus Cadila receives tentative US FDA approval for Ribavirin tablets

Our Corporate Bureau

3 October 2005

Ahmedabad: Zydus Cadila has received tentative approval from the US FDA for

its abbreviated new drug application (ANDA) for Ribavirin tablets, 200mg.

This anti-viral therapy falls in the anti-infectives segment and will go off

patent in December 2005. The current sales of Ribavirin tablets (200 mg) in

the US market as per NDC Health is estimated at $220 million USD.

The tentative approval for Ribavirin Tablets is the latest in a series of

developments that mark Zydus Cadila's entry in the US generic markets. So

far the group has received seven ANDA approvals. The group recently launched

Atenolol in the US market through its US subsidiary Zydus Pharmaceuticals

USA Inc.

The process of filing ANDAs began in 2003-04 with the group filing 12 ANDAs,

the largest number filed by an Indian company in the very first year of

filing. Till date, the group has filed 27 ANDAs and 32 DMFs.

http://www.domain-b.com/companies/companies_z/zydus/20051003_tentative.html

Link to comment
Share on other sites

Zydus Cadila receives tentative US FDA approval for Ribavirin tablets

Our Corporate Bureau

3 October 2005

Ahmedabad: Zydus Cadila has received tentative approval from the US FDA for

its abbreviated new drug application (ANDA) for Ribavirin tablets, 200mg.

This anti-viral therapy falls in the anti-infectives segment and will go off

patent in December 2005. The current sales of Ribavirin tablets (200 mg) in

the US market as per NDC Health is estimated at $220 million USD.

The tentative approval for Ribavirin Tablets is the latest in a series of

developments that mark Zydus Cadila's entry in the US generic markets. So

far the group has received seven ANDA approvals. The group recently launched

Atenolol in the US market through its US subsidiary Zydus Pharmaceuticals

USA Inc.

The process of filing ANDAs began in 2003-04 with the group filing 12 ANDAs,

the largest number filed by an Indian company in the very first year of

filing. Till date, the group has filed 27 ANDAs and 32 DMFs.

http://www.domain-b.com/companies/companies_z/zydus/20051003_tentative.html

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...