Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.
01 2ATHENA
02 4DR REDDYS LABS SA
03 7ACTAVIS ELIZABETH
04 3ACTAVIS LABS UT INC
05 1AJANTA PHARMA LTD
06 3ALEMBIC PHARMS LTD
07 2AM REGENT
08 3AM THERAP
09 1AMNEAL PHARMS NY
10 3AUROBINDO PHARMA LTD
11 6BOEHRINGER INGELHEIM
12 3CHARTWELL MOLECULES
13 1CHARTWELL RX
14 4CONCORDIA PHARMS INC
15 3DIFGEN PHARMS
16 3DURAMED PHARMS BARR
17 4ENDO OPERATIONS
18 2FRESENIUS KABI USA
19 2HIKMA FARMACEUTICA
20 3IMPAX LABS
21 3INTERPHARM
22 1JUBILANT GENERICS
23 3LAVIPHARM
24 2MYLAN INSTITUTIONAL
25 3MYLAN TECHNOLOGIES
26 3NATCO PHARMA
27 1NOVAST LABS
28 6PAR PHARM
29 3PRINSTON INC
30 3RISING
31 1SOMERSET THERAPS LLC
32 3SUN PHARM INDS INC
33 3TEVA
34 2TRIS PHARMA INC
35 3TRUPHARMA
36 3UNICHEM
37 3WARNER CHILCOTT
38 6WATSON LABS
39 2XGEN PHARMS
40 1XIAMEN LP PHARM CO
41 3YUNG SHIN PHARM
42 2ZYDUS PHARMS
01 12INJECTABLE;INJECTION
02 2SUSPENSION, EXTENDED RELEASE;ORAL
03 15SYSTEM;TRANSDERMAL
04 22TABLET, EXTENDED RELEASE;ORAL
05 69TABLET;ORAL
01 61DISCN
02 59RX
01 3CATAPRES
02 1CATAPRES-TTS-1
03 1CATAPRES-TTS-2
04 1CATAPRES-TTS-3
05 13CLONIDINE
06 83CLONIDINE HYDROCHLORIDE
07 3CLONIDINE HYDROCHLORIDE AND CHLORTHALIDONE
08 3CLORPRES
09 3COMBIPRES
10 2DURACLON
11 2JENLOGA
12 2KAPVAY
13 2NEXICLON XR
14 1ONYDA XR
01 104No
02 16Yes
RLD : No
TE Code :
Brand Name : NEXICLON XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 0.17MG BASE
Approval Date : 2009-12-03
Application Number : 22500
RX/OTC/DISCN : RX
RLD : No
TE Code :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : CLONIDINE
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.1MG/24HR
Approval Date : 2010-08-20
Application Number : 79090
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : NEXICLON XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 0.26MG BASE
Approval Date : 2009-12-03
Application Number : 22500
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : CLONIDINE
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.2MG/24HR
Approval Date : 2010-08-20
Application Number : 79090
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : CLONIDINE
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.3MG/24HR
Approval Date : 2010-08-20
Application Number : 79090
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code :
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 0.1MG
Approval Date : 2018-04-30
Application Number : 210680
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : CATAPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17407
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : CATAPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17407
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : CATAPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17407
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Brand Name : COMBIPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG;0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17503
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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