01 3ALOGLIPTIN BENZOATE
02 2ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE
03 6ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE
04 1AMOXICILLIN; CLARITHROMYCIN; LANSOPRAZOLE
05 10AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
06 2ANAGRELIDE HYDROCHLORIDE
07 1BORTEZOMIB
08 3BRIGATINIB
09 1BUDESONIDE
10 3CARBAMAZEPINE
11 1CEFOTIAM HYDROCHLORIDE
12 1CICLESONIDE
13 1COLCHICINE
14 3DEXLANSOPRAZOLE
15 1ECALLANTIDE
16 2FEBUXOSTAT
17 2FRUQUINTINIB
18 2GLIMEPIRIDE; PIOGLITAZONE HYDROCHLORIDE
19 4GUANFACINE HYDROCHLORIDE
20 1ICATIBANT ACETATE
21 3IXAZOMIB CITRATE
22 2LANADELUMAB-FLYO
23 7LANSOPRAZOLE
24 3LANSOPRAZOLE; NAPROXEN
25 6LANTHANUM CARBONATE
26 13LISDEXAMFETAMINE DIMESYLATE
27 1MARIBAVIR
28 3MESALAMINE
29 4METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
30 3MIDODRINE HYDROCHLORIDE
31 1MOBOCERTINIB SUCCINATE
32 8PEGINESATIDE ACETATE
33 3PIOGLITAZONE HYDROCHLORIDE
34 4PONATINIB HYDROCHLORIDE
35 2PRUCALOPRIDE SUCCINATE
36 1RAMELTEON
37 1TEDUGLUTIDE
38 5VEDOLIZUMAB
39 4VORTIOXETINE HYDROBROMIDE
01 3CAPSULE, DELAYED REL PELLETS, TABLET;ORAL
02 2CAPSULE, DELAYED REL PELLETS;ORAL
03 2CAPSULE, DELAYED RELEASE;ORAL
04 15CAPSULE, EXTENDED RELEASE;ORAL
05 1CAPSULE, TABLET, CAPSULE, DELAYED REL PELLETS;ORAL
06 15CAPSULE;ORAL
07 2FOR SUSPENSION, DELAYED RELEASE;ORAL
08 1INJECTABLE; INJECTION
09 3INJECTABLE;INJECTION
10 3INJECTABLE;INTRAVENOUS
11 1INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
12 2INJECTABLE;SUBCUTANEOUS
13 2POWDER;ORAL
14 1POWDER;SUBCUTANEOUS
15 8SOLUTION;INTRAVENOUS, SUBCUTANEOUS
16 2SOLUTION;SUBCUTANEOUS
17 1SPRAY; NASAL
18 1SUSPENSION;ORAL
19 10TABLET, CHEWABLE;ORAL
20 1TABLET, DELAYED RELEASE;ORAL
21 6TABLET, EXTENDED RELEASE;ORAL
22 3TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE;ORAL
23 39TABLET;ORAL
01 10.6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 11.25MG;1.25MG;1.25MG;1.25MG
03 11.2GM
04 1100MG
05 2108MG/0.68ML
06 210MG
07 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 110MG/ML
09 112.5MG;12.5MG;12.5MG;12.5MG
10 115MG
11 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 115MG,N/A;N/A,250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
13 115MG,N/A;N/A,375MG
14 115MG,N/A;N/A,500MG
15 115MG/PACKET
16 1180MG
17 11GM;EQ 15MG BASE
18 11GM;EQ 30MG BASE
19 11MG
20 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 12.5MG;2.5MG;2.5MG;2.5MG
22 2200MG
23 220MG
24 1250MG
25 12MG/10ML
26 12MG;30MG
27 13.125MG;3.125MG;3.125MG;3.125MG
28 13.5MG/VIAL
29 13.75MG;3.75MG;3.75MG;3.75MG
30 4300MG
31 2300MG/2ML (150MG/ML)
32 730MG
33 130MG/PACKET
34 130MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 340MG
36 14MG;30MG
37 1500MG
38 1500MG;500MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
39 1500MG;EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
40 150MCG
41 250MG
42 15MG
43 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
44 15MG/VIAL
45 15MG;5MG;5MG;5MG
46 26.25MG;6.25MG;6.25MG;6.25MG
47 360MG
48 17.5MG;7.5MG;7.5MG;7.5MG
49 170MG
50 180MG
51 1850MG;EQ 15MG BASE
52 18MG
53 19.375MG;9.375MG;9.375MG;9.375MG
54 190MG
55 1EQ 0.5MG BASE
56 2EQ 10MG BASE
57 1EQ 10MG BASE/ML (EQ 10MG BASE/ML)
58 1EQ 12.5MG BASE
59 1EQ 12.5MG BASE;1GM
60 1EQ 12.5MG BASE;500MG
61 1EQ 12.5MG BASE;EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 1EQ 12.5MG BASE;EQ 30MG BASE
63 1EQ 12.5MG BASE;EQ 45MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
64 2EQ 15MG BASE
65 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
66 2EQ 1GM BASE
67 1EQ 1GM BASE/VIAL
68 2EQ 1MG BASE
69 1EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 1EQ 1MG BASE/0.5ML (EQ 1MG BASE/0.5ML)
71 1EQ 2.3MG BASE
72 1EQ 20MG BASE
73 1EQ 20MG BASE/2ML (EQ 10MG BASE/ML)
74 1EQ 250MG BASE
75 1EQ 25MG BASE
76 1EQ 25MG BASE;EQ 15MG BASE
77 1EQ 25MG BASE;EQ 30MG BASE
78 1EQ 25MG BASE;EQ 45MG BASE
79 2EQ 2MG BASE
80 1EQ 2MG BASE/0.5ML (EQ 2MG BASE/0.5ML)
81 2EQ 30MG BASE
82 1EQ 30MG BASE/3ML (EQ 10MG BASE/ML)
83 2EQ 3MG BASE
84 1EQ 3MG BASE/0.5ML (EQ 3MG BASE/0.5ML)
85 1EQ 40MG BASE
86 2EQ 45MG BASE
87 2EQ 4MG BASE
88 1EQ 4MG BASE/0.5ML (EQ 4MG BASE/0.5ML)
89 1EQ 500MG BASE
90 1EQ 5MG BASE
91 1EQ 5MG BASE/0.5ML (EQ 5MG BASE/0.5ML)
92 1EQ 6.25MG BASE
93 1EQ 6MG BASE/0.5ML (EQ 6MG BASE/0.5ML)
94 2EQ 750MG BASE
01 31DISCN
02 84RX
03 9Blank
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NESINA
Dosage Strength : EQ 6.25MG BASE
Approval Date : 2013-01-25
Application Number : 22271
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NESINA
Dosage Strength : EQ 12.5MG BASE
Approval Date : 2013-01-25
Application Number : 22271
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NESINA
Dosage Strength : EQ 25MG BASE
Approval Date : 2013-01-25
Application Number : 22271
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : KAZANO
Dosage Strength : EQ 12.5MG BASE;500MG
Approval Date : 2013-01-25
Application Number : 203414
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : KAZANO
Dosage Strength : EQ 12.5MG BASE;1GM
Approval Date : 2013-01-25
Application Number : 203414
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : OSENI
Dosage Strength : EQ 25MG BASE;EQ 15MG BAS...
Approval Date : 2013-01-25
Application Number : 22426
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : OSENI
Dosage Strength : EQ 25MG BASE;EQ 30MG BAS...
Approval Date : 2013-01-25
Application Number : 22426
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : OSENI
Dosage Strength : EQ 25MG BASE;EQ 45MG BAS...
Approval Date : 2013-01-25
Application Number : 22426
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : OSENI
Dosage Strength : EQ 12.5MG BASE;EQ 15MG B...
Approval Date : 2013-01-25
Application Number : 22426
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : OSENI
Dosage Strength : EQ 12.5MG BASE;EQ 30MG B...
Approval Date : 2013-01-25
Application Number : 22426
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
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