loader
Please Wait
Applying Filters...

Bora CDMO Bora CDMO

X

Approved Drug Products containing 20741 listed in the FDA Orange Book. Original Data : FDA Website

Client Virtual Booth
Menu
Left Arrow
Right Arrow
Filters Filter
Cross PopUp
FILTER :

filter

01 GEMINI LABS LLC (3)

filter

01 TABLET;ORAL (3)

filter

01 DISCN (3)

filter

01 PRANDIN (3)

filter

01 Yes (3)

URL Supplier Web Content
TABLET; ORAL
1MG **Federal Regi...
1997-12-22
20741
PRANDIN
DISCN
Yes
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
URL Supplier Web Content
TABLET; ORAL
2MG **Federal Regi...
1997-12-22
20741
PRANDIN
DISCN
Yes
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
URL Supplier Web Content
TABLET; ORAL
0.5MG **Federal Re...
1997-12-22
20741
PRANDIN
DISCN
Yes
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for FDA Orange Book APPLICATION 20741

Looking for FDA Orange Book APPLICATION 20741 3

19

GEMINI PACKAGING LTD, based in Canada, is a pharmaceutical company.

One of their notable products is REPAGLINIDE, with a corresponding application number 20741.

Regulatory Information DISCN

With a dosage strength 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Dosage Form Route TABLET; ORAL

Reference Listed Drug Yes

Approved since 1997-12-22

18

GEMINI PACKAGING LTD, based in Canada, is a pharmaceutical company.

One of their notable products is REPAGLINIDE, with a corresponding application number 20741.

Regulatory Information DISCN

With a dosage strength 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Dosage Form Route TABLET; ORAL

Reference Listed Drug Yes

Approved since 1997-12-22

17

GEMINI PACKAGING LTD, based in Canada, is a pharmaceutical company.

One of their notable products is REPAGLINIDE, with a corresponding application number 20741.

Regulatory Information DISCN

With a dosage strength 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Dosage Form Route TABLET; ORAL

Reference Listed Drug Yes

Approved since 1997-12-22

Post Enquiry
POST ENQUIRY