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01 4LEVETIRACETAM
02 2LIDOCAINE HYDROCHLORIDE
03 3NITROGLYCERIN
04 1PROCHLORPERAZINE EDISYLATE
05 2VARENICLINE TARTRATE
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 : LIDOCAINE HYDROCHLORIDE
Dosage Strength : 1%
Approval Date : 2026-03-19
Application Number : 220071
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : LIDOCAINE HYDROCHLORIDE
Dosage Strength : 2%
Approval Date : 2026-03-19
Application Number : 220071
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
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
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