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01 4LEVETIRACETAM
02 2LIDOCAINE HYDROCHLORIDE
03 3NITROGLYCERIN
04 1PROCHLORPERAZINE EDISYLATE
05 2VARENICLINE TARTRATE
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01 3INJECTABLE;INJECTION
02 6TABLET;ORAL
03 3TABLET;SUBLINGUAL
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01 10.3MG
02 10.4MG
03 10.6MG
04 11%
05 11GM
06 12%
07 1250MG
08 1500MG
09 1750MG
10 1EQ 0.5MG BASE
11 1EQ 1MG BASE
12 1EQ 5MG BASE/ML
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01 10RX
02 2Blank
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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

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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

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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

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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

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RLD :
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : LIDOCAINE HYDROCHLORIDE
Dosage Strength : 1%
Approval Date :
Application Number : 220071
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : LIDOCAINE HYDROCHLORIDE
Dosage Strength : 2%
Approval Date :
Application Number : 220071
RX/OTC/DISCN :
RLD :
TE Code :

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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

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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

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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

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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

Viwit Pharmaceuticals Limited is a supplier offers 16 products (APIs, Excipients or Intermediates).
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