01 1BUPROPION HYDROCHLORIDE; NALTREXONE HYDROCHLORIDE
02 2DOXEPIN HYDROCHLORIDE
03 2NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE
04 1SUMATRIPTAN SUCCINATE
01 1POWDER;NASAL
02 1TABLET, EXTENDED RELEASE;ORAL
03 4TABLET;ORAL
01 1500MG;EQ 85MG BASE
02 160MG;EQ 10MG BASE
03 190MG;8MG
04 1EQ 11MG BASE
05 1EQ 3MG BASE
06 1EQ 6MG BASE
01 1DISCN
02 5RX
RLD : Yes
TE Code :
BUPROPION HYDROCHLORIDE; NALTREXONE HYDROCHLORIDE
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : CONTRAVE
Dosage Strength : 90MG;8MG
Approval Date : 2014-09-10
Application Number : 200063
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SILENOR
Dosage Strength : EQ 3MG BASE
Approval Date : 2010-03-17
Application Number : 22036
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : SILENOR
Dosage Strength : EQ 6MG BASE
Approval Date : 2010-03-17
Application Number : 22036
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE
Dosage Form : TABLET; ORAL
Proprietary Name : TREXIMET
Dosage Strength : 500MG;EQ 85MG BASE
Approval Date : 2008-04-15
Application Number : 21926
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE
Dosage Form : TABLET; ORAL
Proprietary Name : TREXIMET
Dosage Strength : 60MG;EQ 10MG BASE
Approval Date : 2015-05-14
Application Number : 21926
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : POWDER; NASAL
Proprietary Name : ONZETRA XSAIL
Dosage Strength : EQ 11MG BASE
Approval Date : 2016-01-27
Application Number : 206099
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
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