01 3ATENOLOL
02 2ATENOLOL; CHLORTHALIDONE
03 3BUPROPION HYDROCHLORIDE
04 2CHOLINE FENOFIBRATE
05 2CYCLOBENZAPRINE HYDROCHLORIDE
06 2DEXLANSOPRAZOLE
07 1DICLOFENAC SODIUM
08 2DICYCLOMINE HYDROCHLORIDE
09 8DILTIAZEM HYDROCHLORIDE
10 2DIMETHYL FUMARATE
11 1DONEPEZIL HYDROCHLORIDE
12 1FLUOXETINE HYDROCHLORIDE
13 4FLUPHENAZINE HYDROCHLORIDE
14 4GUANFACINE HYDROCHLORIDE
15 6LISINOPRIL
16 1MEGESTROL ACETATE
17 2METFORMIN HYDROCHLORIDE
18 2MYCOPHENOLATE SODIUM
19 3NAPROXEN SODIUM
20 3NIFEDIPINE
21 3OXCARBAZEPINE
22 4POTASSIUM CHLORIDE
23 3PROPAFENONE HYDROCHLORIDE
24 2TERBUTALINE SULFATE
25 2TESTOSTERONE
26 2TOPIRAMATE
01 6CAPSULE, DELAYED RELEASE;ORAL
02 13CAPSULE, EXTENDED RELEASE;ORAL
03 3CAPSULE;ORAL
04 1GEL, METERED;TRANSDERMAL
05 1SOLUTION, METERED;TRANSDERMAL
06 1SOLUTION;TOPICAL
07 1SUSPENSION;ORAL
08 2TABLET, DELAYED RELEASE;ORAL
09 22TABLET, EXTENDED RELEASE;ORAL
10 20TABLET;ORAL
01 11.5%
02 11.62% (20.25MG/1.25GM ACTUATION)
03 1100MG
04 1100MG;25MG
05 210MEQ
06 310MG
07 3120MG
08 1125MG/ML
09 2150MG
10 215MG
11 1180MG
12 11GM
13 11MG
14 32.5MG
15 120MEQ
16 220MG
17 1225MG
18 123MG
19 2240MG
20 225MG
21 3300MG
22 430MG
23 130MG/1.5ML ACTUATION
24 1325MG
25 1360MG
26 140MG
27 1425MG
28 1450MG
29 1500MG
30 150MG
31 150MG;25MG
32 35MG
33 1600MG
34 360MG
35 18MEQ
36 290MG
37 1EQ 135MG FENOFIBRIC ACID
38 1EQ 180MG BASE
39 1EQ 1MG BASE
40 1EQ 2MG BASE
41 1EQ 360MG BASE
42 1EQ 375MG BASE
43 1EQ 3MG BASE
44 1EQ 45MG FENOFIBRIC ACID
45 1EQ 4MG BASE
46 1EQ 500MG BASE
47 1EQ 60MG BASE
48 1EQ 750MG BASE
01 13DISCN
02 54RX
03 3Blank
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TENORMIN
Dosage Strength : 50MG
Approval Date : 1982-01-01
Application Number : 18240
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TENORMIN
Dosage Strength : 100MG
Approval Date : 1982-01-01
Application Number : 18240
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TENORMIN
Dosage Strength : 25MG
Approval Date : 1990-04-09
Application Number : 18240
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TENORETIC 100
Dosage Strength : 100MG;25MG
Approval Date : 1984-06-08
Application Number : 18760
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TENORETIC 50
Dosage Strength : 50MG;25MG
Approval Date : 1984-06-08
Application Number : 18760
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : FORFIVO XL
Dosage Strength : 450MG
Approval Date : 2011-11-10
Application Number : 22497
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AB3
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 150MG
Approval Date : 2017-11-03
Application Number : 210081
RX/OTC/DISCN : RX
RLD : No
TE Code : AB3
RLD : No
TE Code : AB3
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 300MG
Approval Date : 2017-11-03
Application Number : 210081
RX/OTC/DISCN : RX
RLD : No
TE Code : AB3
RLD : No
TE Code :
Dosage Form : CAPSULE, DELAYED RELEASE; ORAL
Proprietary Name : FENOFIBRIC ACID
Dosage Strength : EQ 45MG FENOFIBRIC ACID
Approval Date : 2019-07-05
Application Number : 210469
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE, DELAYED RELEASE; ORAL
Proprietary Name : FENOFIBRIC ACID
Dosage Strength : EQ 135MG FENOFIBRIC ACID
Approval Date : 2019-07-05
Application Number : 210469
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
