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01 1ACETAMINOPHEN
02 1ACETAMINOPHEN; IBUPROFEN
03 4CETIRIZINE HYDROCHLORIDE
04 1ESOMEPRAZOLE MAGNESIUM
05 2FAMOTIDINE
06 3FLUOXETINE HYDROCHLORIDE
07 3GABAPENTIN
08 2GUAIFENESIN
09 6IBUPROFEN
10 2LORATADINE
11 5METFORMIN HYDROCHLORIDE
12 1NAPROXEN SODIUM
13 1OMEPRAZOLE MAGNESIUM
14 3PARICALCITOL
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01 1CAPSULE, DELAYED RELEASE;ORAL
02 11CAPSULE;ORAL
03 1TABLET, DELAYED RELEASE;ORAL
04 5TABLET, EXTENDED RELEASE;ORAL
05 17TABLET;ORAL
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01 11.2GM
02 1100MG
03 510MG
04 11GM
05 11MCG
06 2200MG
07 120MG
08 1220MG
09 1250MG;125MG
10 12MCG
11 1300MG
12 2400MG
13 14MCG
14 2500MG
15 25MG
16 2600MG
17 1650MG
18 1750MG
19 1800MG
20 1850MG
21 1EQ 10MG BASE
22 1EQ 200MG FREE ACID AND POTASSIUM SALT
23 3EQ 20MG BASE
24 1EQ 40MG BASE
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01 17OTC
02 17RX
03 1Blank
RLD : No
TE Code :
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : ACETAMINOPHEN
Dosage Strength : 650MG
Approval Date : 2021-08-25
Application Number : 215486
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND IBUPRO...
Dosage Strength : 250MG;125MG
Approval Date : 2023-07-10
Application Number : 216994
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 5MG
Approval Date : 2010-06-15
Application Number : 78933
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 : 2010-06-15
Application Number : 78933
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 5MG
Approval Date : 2010-06-15
Application Number : 78933
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 : 2010-06-15
Application Number : 78933
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE, DELAYED RELEASE; ORAL
Proprietary Name : 0
Dosage Strength : EQ 20MG BASE
Approval Date : 2023-09-29
Application Number : 217264
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 10MG
Approval Date : 2023-03-08
Application Number : 217543
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 20MG
Approval Date : 2023-03-08
Application Number : 217543
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code : AB1
Dosage Form : CAPSULE; ORAL
Proprietary Name : FLUOXETINE HYDROCHLORIDE
Dosage Strength : EQ 10MG BASE
Approval Date : 2002-01-29
Application Number : 75465
RX/OTC/DISCN : RX
RLD : No
TE Code : AB1
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