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01 1AMOXICILLIN; CLARITHROMYCIN; OMEPRAZOLE
02 2CONIVAPTAN HYDROCHLORIDE
03 1DIPHENHYDRAMINE HYDROCHLORIDE
04 1GRANISETRON
05 2TELAVANCIN HYDROCHLORIDE
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01 1CAPSULE, TABLET, CAPSULE, DELAYED RELEASE;ORAL
02 1FILM, EXTENDED RELEASE;TRANSDERMAL
03 2INJECTABLE;INTRAVENOUS
04 2POWDER;INTRAVENOUS
05 1SYRUP;ORAL
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01 112.5MG/5ML
02 120MG/100ML (0.2MG/ML)
03 120MG/4ML (5MG/ML)
04 13.1MG/24HR
05 1500MG,N/A,N/A;N/A,500MG,N/A;N/A,N/A,20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 1EQ 250MG BASE/VIAL
07 1EQ 750MG BASE/VIAL
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01 4DISCN
02 3RX
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RLD : Yes
TE Code :
AMOXICILLIN; CLARITHROMYCIN; OMEPRAZOLE
Dosage Form : CAPSULE, TABLET, CAPSULE, DELA...
Proprietary Name : OMECLAMOX-PAK
Dosage Strength : 500MG,N/A,N/A;N/A,500MG,...
Approval Date : 2011-02-08
Application Number : 50824
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : No
TE Code :
Dosage Form : INJECTABLE; INTRAVENOUS
Proprietary Name : VAPRISOL
Dosage Strength : 20MG/4ML (5MG/ML)
Approval Date : 2005-12-29
Application Number : 21697
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INTRAVENOUS
Proprietary Name : VAPRISOL IN 5% DEXTROSE ...
Dosage Strength : 20MG/100ML (0.2MG/ML)
Approval Date : 2008-10-08
Application Number : 21697
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : No
TE Code :
Dosage Form : SYRUP; ORAL
Proprietary Name : DIPHENHYDRAMINE HYDROCHL...
Dosage Strength : 12.5MG/5ML
Approval Date : 1992-08-20
Application Number : 73611
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : Yes
TE Code :
Dosage Form : FILM, EXTENDED RELEASE; TRANSD...
Proprietary Name : SANCUSO
Dosage Strength : 3.1MG/24HR
Approval Date : 2008-09-12
Application Number : 22198
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : VIBATIV
Dosage Strength : EQ 250MG BASE/VIAL
Approval Date : 2009-09-11
Application Number : 22110
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : VIBATIV
Dosage Strength : EQ 750MG BASE/VIAL
Approval Date : 2009-09-11
Application Number : 22110
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
