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01 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE
02 7AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
03 5ARMODAFINIL
04 3BENZTROPINE MESYLATE
05 1CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE
06 2DEXTROAMPHETAMINE SULFATE
07 3DIAZEPAM
08 1DICLOFENAC SODIUM
09 1FOLIC ACID
10 3HYDROXYZINE HYDROCHLORIDE
11 2MODAFINIL
12 2NAPROXEN
13 5OXYCODONE HYDROCHLORIDE
14 4PHENTERMINE HYDROCHLORIDE
15 1POLYETHYLENE GLYCOL 3350
16 2SODIUM POLYSTYRENE SULFONATE
17 2SULFASALAZINE
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01 5CAPSULE;ORAL
02 1FOR SOLUTION;ORAL
03 2POWDER;ORAL, RECTAL
04 1SOLUTION;TOPICAL
05 3TABLET, DELAYED RELEASE;ORAL
06 33TABLET;ORAL
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01 10.5MG
02 11.25MG;1.25MG;1.25MG;1.25MG
03 11.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 11.875MG;1.875MG;1.875MG;1.875MG
05 1100MG
06 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 410MG
08 1150MG
09 115GM/BOT
10 215MG
11 117GM/SCOOPFUL
12 21MG
13 12.5MG;2.5MG;2.5MG;2.5MG
14 2200MG
15 120MG
16 1250MG
17 125MG
18 22MG
19 13.125MG;3.125MG;3.125MG;3.125MG
20 13.75MG;3.75MG;3.75MG;3.75MG
21 1300MG;50MG;40MG
22 230MG
23 237.5MG
24 1375MG
25 1454GM/BOT
26 3500MG
27 250MG
28 35MG
29 15MG;2.5MG
30 15MG;5MG;5MG;5MG
31 17.5MG;7.5MG;7.5MG;7.5MG
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01 2DISCN
02 1OTC
03 42RX
RLD : No
TE Code : AA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : CAPSULE; ORAL
Proprietary Name : BUTALBITAL, ACETAMINOPHE...
Dosage Strength : 300MG;50MG;40MG
Approval Date : 2016-10-28
Application Number : 207118
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AB
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROAMP SACCHARATE, AM...
Dosage Strength : 1.25MG;1.25MG;1.25MG;1.2...
Approval Date : 2017-12-28
Application Number : 209799
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROAMP SACCHARATE, AM...
Dosage Strength : 1.875MG;1.875MG;1.875MG;...
Approval Date : 2017-12-28
Application Number : 209799
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROAMP SACCHARATE, AM...
Dosage Strength : 2.5MG;2.5MG;2.5MG;2.5MG
Approval Date : 2017-12-28
Application Number : 209799
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROAMP SACCHARATE, AM...
Dosage Strength : 3.125MG;3.125MG;3.125MG;...
Approval Date : 2017-12-28
Application Number : 209799
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROAMP SACCHARATE, AM...
Dosage Strength : 3.75MG;3.75MG;3.75MG;3.7...
Approval Date : 2017-12-28
Application Number : 209799
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROAMP SACCHARATE, AM...
Dosage Strength : 5MG;5MG;5MG;5MG
Approval Date : 2017-12-28
Application Number : 209799
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROAMP SACCHARATE, AM...
Dosage Strength : 7.5MG;7.5MG;7.5MG;7.5MG
Approval Date : 2017-12-28
Application Number : 209799
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : NUVIGIL
Dosage Strength : 50MG
Approval Date : 2007-06-15
Application Number : 21875
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NUVIGIL
Dosage Strength : 100MG **Federal Register...
Approval Date : 2009-03-26
Application Number : 21875
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :