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01 1CLOFARABINE
02 2ERYTHROMYCIN
03 1GABAPENTIN
04 1SUCRALFATE
05 2VENLAFAXINE HYDROCHLORIDE
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01 7ABON PHARMS LLC
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01 1SOLUTION;INTRAVENOUS
02 1SUSPENSION;ORAL
03 2TABLET, EXTENDED RELEASE;ORAL
04 3TABLET;ORAL
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01 11GM/10ML
02 120MG/20ML (1MG/ML)
03 1250MG
04 1500MG
05 1600MG
06 1EQ 150MG BASE
07 1EQ 225MG BASE
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01 7USA
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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : CLOFARABINE
Dosage Strength : 20MG/20ML (1MG/ML)
Packaging :
Approval Date : 2017-05-09
Application Number : 204029
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ERYTHROMYCIN
Dosage Strength : 250MG
Packaging :
Approval Date : 2025-09-23
Application Number : 219691
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ERYTHROMYCIN
Dosage Strength : 500MG
Packaging :
Approval Date : 2025-09-23
Application Number : 219691
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : GABAPENTIN
Dosage Strength : 600MG
Packaging :
Approval Date : 2024-09-09
Application Number : 203643
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SUSPENSION;ORAL
Brand Name : SUCRALFATE
Dosage Strength : 1GM/10ML
Packaging :
Approval Date : 2024-03-21
Application Number : 216726
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : VENLAFAXINE HYDROCHLORIDE
Dosage Strength : EQ 150MG BASE
Packaging :
Approval Date : 2025-02-07
Application Number : 217841
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : VENLAFAXINE HYDROCHLORIDE
Dosage Strength : EQ 225MG BASE
Packaging :
Approval Date : 2025-02-07
Application Number : 217841
Regulatory Info : RX
Registration Country : USA
