01 2CETIRIZINE HYDROCHLORIDE
02 1CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
03 1CLEMASTINE FUMARATE
04 1DIPHENHYDRAMINE CITRATE; IBUPROFEN
05 1FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
06 1LORATADINE
07 1NAPROXEN SODIUM
08 2NICOTINE POLACRILEX
09 2ZOLMITRIPTAN
01 1TABLET, EXTENDED RELEASE; ORAL
02 1TABLET, EXTENDED RELEASE;ORAL
03 8TABLET;ORAL
04 2TROCHE/LOZENGE;ORAL
01 11.34MG
02 210MG
03 12.5MG
04 1220MG
05 138MG;200MG
06 25MG
07 15MG;120MG
08 160MG; 120MG
09 1EQ 2MG BASE
10 1EQ 4MG BASE
01 2DISCN
02 7OTC
03 2RX
04 1Blank
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 5MG
Approval Date : 2007-12-27
Application Number : 77946
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 10MG
Approval Date : 2007-12-27
Application Number : 77946
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 5MG;120MG
Approval Date : 2008-03-05
Application Number : 77991
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CLEMASTINE FUMARATE
Dosage Strength : 1.34MG
Approval Date : 1993-10-31
Application Number : 73458
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
DIPHENHYDRAMINE CITRATE; IBUPROFEN
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN AND DIPHENHYDR...
Dosage Strength : 38MG;200MG
Approval Date : 2024-04-11
Application Number : 211404
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD :
TE Code :
FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : TABLET, EXTENDED RELEASE; ORA...
Proprietary Name : FEXOFENADINE HYDROCHLORI...
Dosage Strength : 60MG; 120MG
Approval Date :
Application Number : 77999
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : LORATADINE
Dosage Strength : 10MG
Approval Date : 2003-01-21
Application Number : 75209
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NAPROXEN SODIUM
Dosage Strength : 220MG
Approval Date : 1997-01-13
Application Number : 74646
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TROCHE/LOZENGE; ORAL
Proprietary Name : NICOTINE POLACRILEX
Dosage Strength : EQ 2MG BASE
Approval Date : 2019-02-07
Application Number : 207868
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TROCHE/LOZENGE; ORAL
Proprietary Name : NICOTINE POLACRILEX
Dosage Strength : EQ 4MG BASE
Approval Date : 2019-02-07
Application Number : 207868
RX/OTC/DISCN : OTC
RLD : No
TE Code :
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