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01 1ACAMPROSATE CALCIUM
02 3BUMETANIDE
03 2CHLORTHALIDONE
04 1CLINDAMYCIN PALMITATE HYDROCHLORIDE
05 1CLOMIPHENE CITRATE
06 1CYPROHEPTADINE HYDROCHLORIDE
07 5DOXEPIN HYDROCHLORIDE
08 2FLUVOXAMINE MALEATE
09 2GLYCOPYRROLATE
10 6HALOPERIDOL
11 3HYDROCORTISONE
12 4HYDROXYCHLOROQUINE SULFATE
13 4LABETALOL HYDROCHLORIDE
14 2MODAFINIL
15 4PERPHENAZINE
16 3PRAZOSIN HYDROCHLORIDE
17 2PRUCALOPRIDE SUCCINATE
18 1RAMELTEON
19 2RANITIDINE HYDROCHLORIDE
20 5SERTRALINE HYDROCHLORIDE
21 3SILDENAFIL CITRATE
22 1TRANEXAMIC ACID
23 1VALGANCICLOVIR HYDROCHLORIDE
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01 2CAPSULE, EXTENDED RELEASE;ORAL
02 12CAPSULE;ORAL
03 2FOR SOLUTION;ORAL
04 1TABLET, DELAYED RELEASE;ORAL
05 42TABLET;ORAL
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01 20.5MG
02 4100MG
03 210MG
04 1150MG
05 116MG
06 31MG
07 3200MG
08 220MG
09 125MG
10 42MG
11 2300MG
12 1333MG
13 2400MG
14 24MG
15 250MG
16 150MG/ML
17 25MG
18 1650MG
19 28MG
20 3EQ 100MG BASE
21 1EQ 10MG BASE
22 2EQ 150MG BASE
23 2EQ 1MG BASE
24 1EQ 200MG BASE
25 3EQ 25MG BASE
26 2EQ 2MG BASE
27 1EQ 300MG BASE
28 3EQ 50MG BASE
29 1EQ 5MG BASE
30 1EQ 75MG BASE
31 1EQ 75MG BASE/5ML
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01 5DISCN
02 54RX
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RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : ACAMPROSATE CALCIUM
Dosage Strength : 333MG
Approval Date : 2026-03-16
Application Number : 218984
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 : 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 : AA
CLINDAMYCIN PALMITATE HYDROCHLORIDE
Dosage Form : FOR SOLUTION; ORAL
Proprietary Name : CLINDAMYCIN PALMITATE HY...
Dosage Strength : EQ 75MG BASE/5ML
Approval Date : 2018-05-11
Application Number : 207047
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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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
