01 4LEVETIRACETAM
02 3NITROGLYCERIN
03 1PROCHLORPERAZINE EDISYLATE
04 3SERTRALINE HYDROCHLORIDE
05 4TOPIRAMATE
01 1INJECTABLE;INJECTION
02 11TABLET;ORAL
03 3TABLET;SUBLINGUAL
01 10.3MG
02 10.4MG
03 10.6MG
04 1100MG
05 11GM
06 1200MG
07 1250MG
08 125MG
09 1500MG
10 150MG
11 1750MG
12 1EQ 100MG BASE
13 1EQ 25MG BASE
14 1EQ 50MG BASE
15 1EQ 5MG BASE/ML
01 15RX
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 : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : NITROGLYCERIN
Dosage Strength : 0.3MG
Approval Date : 2024-10-15
Application Number : 218583
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : NITROGLYCERIN
Dosage Strength : 0.4MG
Approval Date : 2024-10-15
Application Number : 218583
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : NITROGLYCERIN
Dosage Strength : 0.6MG
Approval Date : 2024-10-15
Application Number : 218583
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
Viwit Pharmaceuticals Limited is a supplier offers 45 products (APIs, Excipients or Intermediates).
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