01 3AMLODIPINE BESYLATE
02 3ARMODAFINIL
03 4BENAZEPRIL HYDROCHLORIDE
04 4CAPTOPRIL
05 1CHLORDIAZEPOXIDE HYDROCHLORIDE; CLIDINIUM BROMIDE
06 4CHLORZOXAZONE
07 3CLORAZEPATE DIPOTASSIUM
08 3DEMECLOCYCLINE HYDROCHLORIDE
09 7DEXAMETHASONE
10 6DEXTROAMPHETAMINE SACCHARATE;AMPHETAMINE ASPARTATE MONOHYDRATE;DEXTROAMPHETAMINE SULFATE;AMPHETAMINE SULFATE
11 2DICYCLOMINE HYDROCHLORIDE
12 1DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
13 3HYDROCHLOROTHIAZIDE; LISINOPRIL
14 6LISINOPRIL
15 3LOVASTATIN
16 2MELOXICAM
17 3PIOGLITAZONE HYDROCHLORIDE
18 4RAMIPRIL
19 3SUMATRIPTAN SUCCINATE
01 6CAPSULE, EXTENDED RELEASE;ORAL
02 6CAPSULE;ORAL
03 53TABLET;ORAL
01 10.5MG
02 10.75MG
03 11.25MG
04 11.5MG
05 1100MG
06 610MG
07 112.5MG
08 112.5MG;10MG
09 112.5MG;20MG
10 1150MG
11 1150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 315MG
13 11MG
14 22.5MG
15 520MG
16 2250MG
17 225MG
18 125MG;20MG
19 125MG;220MG
20 12MG
21 13.75MG
22 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 230MG
24 1375MG
25 340MG
26 14MG
27 1500MG
28 250MG
29 45MG
30 15MG;2.5MG
31 16MG
32 27.5MG
33 1750MG
34 175MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 1EQ 100MG BASE
36 1EQ 10MG BASE
37 1EQ 15MG BASE
38 1EQ 2.5MG BASE
39 1EQ 25MG BASE
40 1EQ 30MG BASE
41 1EQ 45MG BASE
42 1EQ 50MG BASE
43 1EQ 5MG BASE
01 6DISCN
02 1OTC
03 52RX
04 6Blank
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 2.5MG BASE
Approval Date : 2007-05-23
Application Number : 76719
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 5MG BASE
Approval Date : 2007-05-23
Application Number : 76719
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 10MG BASE
Approval Date : 2007-05-23
Application Number : 76719
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ARMODAFINIL
Dosage Strength : 50MG
Approval Date : 2019-03-25
Application Number : 201514
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ARMODAFINIL
Dosage Strength : 150MG
Approval Date : 2019-03-25
Application Number : 201514
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ARMODAFINIL
Dosage Strength : 250MG
Approval Date : 2019-03-25
Application Number : 201514
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BENAZEPRIL HYDROCHLORIDE
Dosage Strength : 5MG
Approval Date : 2006-03-08
Application Number : 77128
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BENAZEPRIL HYDROCHLORIDE
Dosage Strength : 10MG
Approval Date : 2006-03-08
Application Number : 77128
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BENAZEPRIL HYDROCHLORIDE
Dosage Strength : 20MG
Approval Date : 2006-03-08
Application Number : 77128
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BENAZEPRIL HYDROCHLORIDE
Dosage Strength : 40MG
Approval Date : 2006-03-08
Application Number : 77128
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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