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01 1AMOXICILLIN; CLARITHROMYCIN; OMEPRAZOLE
02 2CONIVAPTAN HYDROCHLORIDE
03 1DIPHENHYDRAMINE HYDROCHLORIDE
04 1GRANISETRON
05 2TELAVANCIN HYDROCHLORIDE
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01 6CUMBERLAND
02 1CUMBERLAND SWAN
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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05 1500MG,N/A,N/A;N/A,500MG,N/A;N/A,N/A,20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 7USA
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Regulatory Info : DISCN
Registration Country : USA
AMOXICILLIN; CLARITHROMYCIN; OMEPRAZOLE
Dosage Form : CAPSULE, TABLET, CAPSULE...
Brand Name : OMECLAMOX-PAK
Dosage Strength : 500MG,N/A,N/A;N/A,500M...
Packaging :
Approval Date : 2011-02-08
Application Number : 50824
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : VAPRISOL
Dosage Strength : 20MG/4ML (5MG/ML)
Packaging :
Approval Date : 2005-12-29
Application Number : 21697
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : VAPRISOL IN 5% DEXTROSE I...
Dosage Strength : 20MG/100ML (0.2MG/ML)
Packaging :
Approval Date : 2008-10-08
Application Number : 21697
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SYRUP;ORAL
Brand Name : DIPHENHYDRAMINE HYDROCHLO...
Dosage Strength : 12.5MG/5ML
Packaging :
Approval Date : 1992-08-20
Application Number : 73611
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : FILM, EXTENDED RELEASE;T...
Brand Name : SANCUSO
Dosage Strength : 3.1MG/24HR
Packaging :
Approval Date : 2008-09-12
Application Number : 22198
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : VIBATIV
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 2009-09-11
Application Number : 22110
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : VIBATIV
Dosage Strength : EQ 750MG BASE/VIAL
Packaging :
Approval Date : 2009-09-11
Application Number : 22110
Regulatory Info : RX
Registration Country : USA
