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01 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE
02 1ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
03 1DEXAMETHASONE
04 4FENOPROFEN CALCIUM
05 1VORAPAXAR SULFATE
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01 5CAPSULE;ORAL
02 3TABLET;ORAL
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01 11.5MG
02 1300MG;50MG;40MG
03 1320.5MG;30MG;16MG
04 1EQ 2.08MG BASE
05 1EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 1EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 1EQ 600MG BASE
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01 8DISCN
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RLD : No
TE Code :
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : CAPSULE; ORAL
Proprietary Name : BUTALBITAL, ACETAMINOPHE...
Dosage Strength : 300MG;50MG;40MG
Approval Date : 2017-08-04
Application Number : 206615
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Dosage Form : CAPSULE; ORAL
Proprietary Name : TREZIX
Dosage Strength : 320.5MG;30MG;16MG
Approval Date : 2014-11-26
Application Number : 204785
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DEXAMETHASONE
Dosage Strength : 1.5MG
Approval Date : 1983-04-28
Application Number : 88237
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : NALFON
Dosage Strength : EQ 300MG BASE **Federal ...
Approval Date : 1982-01-01
Application Number : 17604
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : NALFON
Dosage Strength : EQ 200MG BASE **Federal ...
Approval Date : 1982-01-01
Application Number : 17604
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : NALFON
Dosage Strength : EQ 400MG BASE **Federal ...
Approval Date : 2009-07-21
Application Number : 17604
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FENOPROFEN CALCIUM
Dosage Strength : EQ 600MG BASE
Approval Date : 1988-08-17
Application Number : 72267
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ZONTIVITY
Dosage Strength : EQ 2.08MG BASE
Approval Date : 2014-05-08
Application Number : 204886
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
