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01 1ADAPALENE
02 1CLOTRIMAZOLE
03 1DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
04 1DOCOSANOL
05 1ESOMEPRAZOLE MAGNESIUM
06 1FAMOTIDINE
07 3FEXOFENADINE HYDROCHLORIDE
08 1IBUPROFEN
09 1LORATADINE; PSEUDOEPHEDRINE SULFATE
10 1MICONAZOLE NITRATE
11 4MINOXIDIL
12 30NICOTINE POLACRILEX
13 1OMEPRAZOLE MAGNESIUM
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01 2AEROSOL, FOAM;TOPICAL
02 1CREAM;TOPICAL
03 2CREAM;VAGINAL
04 1GEL;TOPICAL
05 14GUM, CHEWING;BUCCAL
06 2SOLUTION;TOPICAL
07 4SUSPENSION;ORAL
08 2TABLET, DELAYED RELEASE;ORAL
09 1TABLET, EXTENDED RELEASE;ORAL
10 2TABLET;ORAL
11 16TROCHE/LOZENGE;ORAL
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01 10.1%
02 11%
03 110%
04 1100MG/5ML
05 110MG
06 110MG;240MG
07 22%
08 125MG;220MG
09 330MG/5ML
10 35%
11 2EQ 20MG BASE
12 15EQ 2MG BASE
13 15EQ 4MG BASE
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01 3DISCN
02 42OTC
03 2Blank
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RLD : No
TE Code :
Dosage Form : GEL; TOPICAL
Proprietary Name : ADAPALENE
Dosage Strength : 0.1%
Approval Date : 2010-06-02
Application Number : 90962
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : CREAM; VAGINAL
Proprietary Name : CLOTRIMAZOLE
Dosage Strength : 1%
Approval Date : 1993-07-16
Application Number : 74165
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
Dosage Form : TABLET; ORAL
Proprietary Name : NAPROXEN SODIUM AND DIPH...
Dosage Strength : 25MG;220MG
Approval Date : 2019-01-25
Application Number : 207597
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : DOCOSANOL
Dosage Strength : 10%
Approval Date : 2018-11-19
Application Number : 208754
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : ESOMEPRAZOLE MAGNESIUM
Dosage Strength : EQ 20MG BASE
Approval Date : 2019-03-05
Application Number : 209202
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 10MG
Approval Date : 2001-07-26
Application Number : 75512
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : FEXOFENADINE HYDROCHLORI...
Dosage Strength : 30MG/5ML
Approval Date : 2012-07-25
Application Number : 201311
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : CHILDRENS FEXOFENADINE H...
Dosage Strength : 30MG/5ML
Approval Date : 2014-11-18
Application Number : 203330
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : CHILDRENS FEXOFENADINE H...
Dosage Strength : 30MG/5ML
Approval Date : 2014-11-18
Application Number : 203330
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 100MG/5ML
Approval Date : 1999-04-30
Application Number : 74916
RX/OTC/DISCN : OTC
RLD : No
TE Code :
