01 1CHLORPROMAZINE HYDROCHLORIDE
02 1CLOTRIMAZOLE
03 4FLUCONAZOLE
04 3MIDODRINE HYDROCHLORIDE
05 2RANITIDINE HYDROCHLORIDE
06 2TINIDAZOLE
01 1INJECTABLE;INJECTION
02 11TABLET;ORAL
03 1TROCHE/LOZENGE;ORAL
01 1100MG
02 210MG
03 1150MG
04 12.5MG
05 1200MG
06 1250MG
07 125MG/ML
08 1500MG
09 150MG
10 15MG
11 1EQ 150MG BASE
12 1EQ 75MG BASE
01 2DISCN
02 11RX
RLD : No
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : CHLORPROMAZINE HYDROCHLO...
Dosage Strength : 25MG/ML
Approval Date : 2024-12-10
Application Number : 216724
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AB
Dosage Form : TROCHE/LOZENGE; ORAL
Proprietary Name : CLOTRIMAZOLE
Dosage Strength : 10MG
Approval Date : 2024-02-29
Application Number : 215641
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FLUCONAZOLE
Dosage Strength : 50MG
Approval Date : 2005-09-28
Application Number : 76957
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FLUCONAZOLE
Dosage Strength : 100MG
Approval Date : 2005-09-28
Application Number : 76957
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FLUCONAZOLE
Dosage Strength : 200MG
Approval Date : 2005-09-28
Application Number : 76957
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FLUCONAZOLE
Dosage Strength : 150MG
Approval Date : 2017-02-27
Application Number : 76957
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MIDODRINE HYDROCHLORIDE
Dosage Strength : 2.5MG
Approval Date : 2018-11-02
Application Number : 207613
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MIDODRINE HYDROCHLORIDE
Dosage Strength : 5MG
Approval Date : 2018-11-02
Application Number : 207613
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MIDODRINE HYDROCHLORIDE
Dosage Strength : 10MG
Approval Date : 2018-11-02
Application Number : 207613
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : RANITIDINE HYDROCHLORIDE
Dosage Strength : EQ 150MG BASE
Approval Date : 2019-08-30
Application Number : 210228
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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