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01 1ALBENDAZOLE
02 1ATROPINE SULFATE
03 3BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
04 6BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
05 1CARBIDOPA
06 1COLESTIPOL HYDROCHLORIDE
07 4DILTIAZEM HYDROCHLORIDE
08 2GLYCOPYRROLATE
09 1IVERMECTIN
10 1LOPERAMIDE HYDROCHLORIDE
11 1MIGLUSTAT
12 4PREDNISOLONE SODIUM PHOSPHATE
13 2TINIDAZOLE
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01 2CAPSULE;ORAL
02 1SOLUTION/DROPS;OPHTHALMIC
03 4SOLUTION;ORAL
04 2TABLET, ORALLY DISINTEGRATING;ORAL
05 13TABLET;ORAL
06 6TABLET;SUBLINGUAL
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01 10.85MG
02 11%
03 11.7MG
04 1100MG
05 110MG;6.25MG
06 1120MG
07 11GM
08 12.5MG;6.25MG
09 1200MG
10 1250MG
11 125MG
12 12MG
13 130MG
14 13MG
15 1500MG
16 15MG;6.25MG
17 160MG
18 190MG
19 1EQ 0.7MG BASE;EQ 0.18MG BASE
20 1EQ 1.4MG BASE;EQ 0.36MG BASE
21 1EQ 10MG BASE/5ML
22 1EQ 11.4MG BASE;EQ 2.9MG BASE
23 1EQ 15MG BASE/5ML
24 1EQ 2.9MG BASE;EQ 0.71MG BASE
25 1EQ 20MG BASE/5ML
26 1EQ 25MG BASE/5ML
27 1EQ 5.7MG BASE;EQ 1.4MG BASE
28 1EQ 8.6MG BASE;EQ 2.1MG BASE
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01 6DISCN
02 21RX
03 1Blank
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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALBENDAZOLE
Dosage Strength : 200MG
Approval Date : 2019-05-14
Application Number : 211117
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD :
TE Code :
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : ATROPINE SULFATE
Dosage Strength : 1%
Approval Date :
Application Number : 219013
RX/OTC/DISCN :
RLD :
TE Code :

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RLD : No
TE Code : AB
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : BISOPROLOL FUMARATE AND ...
Dosage Strength : 2.5MG;6.25MG
Approval Date : 2020-07-09
Application Number : 212678
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : BISOPROLOL FUMARATE AND ...
Dosage Strength : 5MG;6.25MG
Approval Date : 2020-07-09
Application Number : 212678
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : BISOPROLOL FUMARATE AND ...
Dosage Strength : 10MG;6.25MG
Approval Date : 2020-07-09
Application Number : 212678
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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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 :
