01 4LEVETIRACETAM
02 1PROCHLORPERAZINE EDISYLATE
03 3SERTRALINE HYDROCHLORIDE
04 4TOPIRAMATE
01 1INJECTABLE;INJECTION
02 11TABLET;ORAL
01 1100MG
02 11GM
03 1200MG
04 1250MG
05 125MG
06 1500MG
07 150MG
08 1750MG
09 1EQ 100MG BASE
10 1EQ 25MG BASE
11 1EQ 50MG BASE
12 1EQ 5MG BASE/ML
01 12RX
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LEVETIRACETAM
Dosage Strength : 250MG
Approval Date : 2009-03-13
Application Number : 78869
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LEVETIRACETAM
Dosage Strength : 500MG
Approval Date : 2009-03-13
Application Number : 78869
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LEVETIRACETAM
Dosage Strength : 750MG
Approval Date : 2009-03-13
Application Number : 78869
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LEVETIRACETAM
Dosage Strength : 1GM
Approval Date : 2009-03-13
Application Number : 78869
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : PROCHLORPERAZINE EDISYLA...
Dosage Strength : EQ 5MG BASE/ML
Approval Date : 2021-09-28
Application Number : 213626
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SERTRALINE HYDROCHLORIDE
Dosage Strength : EQ 25MG BASE
Approval Date : 2007-02-06
Application Number : 76882
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SERTRALINE HYDROCHLORIDE
Dosage Strength : EQ 50MG BASE
Approval Date : 2007-02-06
Application Number : 76882
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SERTRALINE HYDROCHLORIDE
Dosage Strength : EQ 100MG BASE
Approval Date : 2007-02-06
Application Number : 76882
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TOPIRAMATE
Dosage Strength : 25MG
Approval Date : 2009-03-27
Application Number : 77733
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TOPIRAMATE
Dosage Strength : 50MG
Approval Date : 2009-03-27
Application Number : 77733
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Viwit Pharmaceuticals Limited is a supplier offers 44 products (APIs, Excipients or Intermediates).
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