01 10ABBVIE
02 1ALLERGAN
03 2STRIDES PHARMA
04 2ACME LABS
05 2AJANTA PHARMA LTD
06 2ALEMBIC
07 2ALLIED
08 8AMNEAL PHARMS
09 5ANI PHARMS
10 5APOTEX
11 6AUROBINDO PHARMA LTD
12 2CHARTWELL
13 1CHARTWELL MOLECULAR
14 2DR REDDYS LABS LTD
15 4ENDO OPERATIONS
16 2HETERO LABS LTD V
17 2HIKMA
18 2JUBILANT GENERICS
19 2LANNETT CO INC
20 6LUPIN LTD
21 7MACLEODS PHARMS LTD
22 4NOVAST LABS LTD
23 2ORBION PHARMS
24 2POLYGEN PHARMS
25 2PURACAP PHARM LLC
26 6RISING
27 1SCIEGEN PHARMS INC
28 1SETON PHARMS
29 6SUN PHARM
30 2TEVA PHARMS
31 2TORRENT
32 2UNICHEM
33 2UPSHER SMITH LABS
34 6XIAMEN LP PHARM CO
35 4YICHANG HUMANWELL
36 2YILING
37 2ZYDUS LIFESCIENCES
38 4ZYDUS PHARMS
01 65CAPSULE, EXTENDED RELEASE;ORAL
02 6SOLUTION;ORAL
03 54TABLET;ORAL
01 42DISCN
02 73RX
03 10Blank
01 1DONEPEZIL HYDROCHLORIDE AND MEMANTINE HYDROCHLORIDE
02 108MEMANTINE HYDROCHLORIDE
03 3MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE
04 2MEMANTINE;DONEPEZIL HYDROCHLORIDES
05 3NAMENDA
06 4NAMENDA XR
07 4NAMZARIC
01 104No
02 11Yes
03 10Blank
RLD : Yes
TE Code : AB
Brand Name : NAMENDA
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2003-10-16
Application Number : 21487
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : NAMENDA
Dosage Form : SOLUTION;ORAL
Dosage Strength : 2MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2005-04-18
Application Number : 21627
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Brand Name : MEMANTINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2017-05-23
Application Number : 202350
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : NAMENDA
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 2003-10-16
Application Number : 21487
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : NAMENDA XR
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 7MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2010-06-21
Application Number : 22525
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NAMENDA XR
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 14MG
Approval Date : 2010-06-21
Application Number : 22525
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NAMENDA XR
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 21MG
Approval Date : 2010-06-21
Application Number : 22525
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : NAMENDA XR
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 28MG
Approval Date : 2010-06-21
Application Number : 22525
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE
Brand Name : NAMZARIC
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 10MG;14MG
Approval Date : 2014-12-23
Application Number : 206439
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE
Brand Name : NAMZARIC
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 10MG;28MG
Approval Date : 2014-12-23
Application Number : 206439
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
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