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01 2ATHENA
02 3DR 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 1AZURITY
12 6BOEHRINGER INGELHEIM
13 3CHARTWELL MOLECULES
14 1CHARTWELL RX
15 4CONCORDIA PHARMS INC
16 3DURAMED PHARMS BARR
17 2FRESENIUS KABI USA
18 2HIKMA FARMACEUTICA
19 3IMPAX LABS
20 3INGENUS PHARMS LLC
21 3INTERPHARM
22 1JUBILANT GENERICS
23 3LAVIPHARM
24 2MYLAN INSTITUTIONAL
25 3MYLAN TECHNOLOGIES
26 3NATCO PHARMA
27 1NOVAST LABS
28 6PAR PHARM
29 4PH HEALTH
30 3PRINSTON INC
31 3RISING
32 1RUBICON RESEARCH
33 1SOMERSET THERAPS LLC
34 3SUN PHARM INDS INC
35 3TEVA
36 3TP ANDA HOLDINGS
37 2TRIS PHARMA INC
38 3UNICHEM
39 3WARNER CHILCOTT
40 6WATSON LABS
41 2XGEN PHARMS
42 1XIAMEN LP PHARM CO
43 3YUNG SHIN PHARM
44 2ZYDUS PHARMS
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01 12INJECTABLE;INJECTION
02 1SOLUTION;ORAL
03 2SUSPENSION, EXTENDED RELEASE;ORAL
04 15SYSTEM;TRANSDERMAL
05 22TABLET, EXTENDED RELEASE;ORAL
06 69TABLET;ORAL
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01 63DISCN
02 58RX
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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 1JAVADIN
12 2JENLOGA
13 2KAPVAY
14 2NEXICLON XR
15 1ONYDA XR
01 104No
02 17Yes
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
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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 :

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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 :

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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 :

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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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RLD : Yes
TE Code :
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Brand Name : COMBIPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG;0.2MG **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 :
