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01 6BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
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01 6TABLET;SUBLINGUAL
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01 1EQ 0.7MG BASE;EQ 0.18MG BASE
02 1EQ 1.4MG BASE;EQ 0.36MG BASE
03 1EQ 11.4MG BASE;EQ 2.9MG BASE
04 1EQ 2.9MG BASE;EQ 0.71MG BASE
05 1EQ 5.7MG BASE;EQ 1.4MG BASE
06 1EQ 8.6MG BASE;EQ 2.1MG BASE
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01 6RX
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RLD : Yes
TE Code :
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : ZUBSOLV
Dosage Strength : EQ 1.4MG BASE;EQ 0.36MG ...
Approval Date : 2013-07-03
Application Number : 204242
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : ZUBSOLV
Dosage Strength : EQ 5.7MG BASE;EQ 1.4MG B...
Approval Date : 2013-07-03
Application Number : 204242
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : ZUBSOLV
Dosage Strength : EQ 8.6MG BASE;EQ 2.1MG B...
Approval Date : 2014-12-11
Application Number : 204242
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : ZUBSOLV
Dosage Strength : EQ 11.4MG BASE;EQ 2.9MG ...
Approval Date : 2014-12-11
Application Number : 204242
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : ZUBSOLV
Dosage Strength : EQ 2.9MG BASE;EQ 0.71MG ...
Approval Date : 2015-06-04
Application Number : 204242
RX/OTC/DISCN : RX
RLD : Yes
TE Code :

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
RLD : Yes
TE Code :
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : ZUBSOLV
Dosage Strength : EQ 0.7MG BASE;EQ 0.18MG ...
Approval Date : 2016-10-04
Application Number : 204242
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
