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01 1ACAMPROSATE CALCIUM
02 3BUMETANIDE
03 2CHLORTHALIDONE
04 1CLOMIPHENE CITRATE
05 1CYPROHEPTADINE HYDROCHLORIDE
06 5DOXEPIN HYDROCHLORIDE
07 2GLYCOPYRROLATE
08 6HALOPERIDOL
09 3HYDROCORTISONE
10 4HYDROXYCHLOROQUINE SULFATE
11 4LABETALOL HYDROCHLORIDE
12 2MODAFINIL
13 4PERPHENAZINE
14 3PRAZOSIN HYDROCHLORIDE
15 2PRUCALOPRIDE SUCCINATE
16 1RAMELTEON
17 2RANITIDINE HYDROCHLORIDE
18 5SERTRALINE HYDROCHLORIDE
19 3SILDENAFIL CITRATE
20 1TRANEXAMIC ACID
21 1VALGANCICLOVIR HYDROCHLORIDE
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01 12CAPSULE;ORAL
02 1FOR SOLUTION;ORAL
03 1TABLET, DELAYED RELEASE;ORAL
04 42TABLET;ORAL
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01 20.5MG
02 3100MG
03 210MG
04 116MG
05 31MG
06 3200MG
07 220MG
08 125MG
09 42MG
10 2300MG
11 1333MG
12 2400MG
13 24MG
14 250MG
15 150MG/ML
16 25MG
17 1650MG
18 28MG
19 3EQ 100MG BASE
20 1EQ 10MG BASE
21 2EQ 150MG BASE
22 2EQ 1MG BASE
23 1EQ 200MG BASE
24 3EQ 25MG BASE
25 2EQ 2MG BASE
26 1EQ 300MG BASE
27 3EQ 50MG BASE
28 1EQ 5MG BASE
29 1EQ 75MG BASE
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01 5DISCN
02 50RX
03 1Blank
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RLD :
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : ACAMPROSATE CALCIUM
Dosage Strength : 333MG
Approval Date :
Application Number : 218984
RX/OTC/DISCN :
RLD :
TE Code :

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BUMETANIDE
Dosage Strength : 0.5MG
Approval Date : 2024-09-18
Application Number : 212931
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BUMETANIDE
Dosage Strength : 1MG
Approval Date : 2024-09-18
Application Number : 212931
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BUMETANIDE
Dosage Strength : 2MG
Approval Date : 2024-09-18
Application Number : 212931
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CHLORTHALIDONE
Dosage Strength : 25MG
Approval Date : 2018-10-12
Application Number : 210742
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CHLORTHALIDONE
Dosage Strength : 50MG
Approval Date : 2018-10-12
Application Number : 210742
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CLOMIPHENE CITRATE
Dosage Strength : 50MG
Approval Date : 2024-11-08
Application Number : 216739
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : CYPROHEPTADINE HYDROCHLO...
Dosage Strength : 4MG
Approval Date : 2016-11-29
Application Number : 206553
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : DOXEPIN HYDROCHLORIDE
Dosage Strength : EQ 10MG BASE
Approval Date : 2021-04-01
Application Number : 214908
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : DOXEPIN HYDROCHLORIDE
Dosage Strength : EQ 25MG BASE
Approval Date : 2021-04-01
Application Number : 214908
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
