01 1ABACAVIR SULFATE; LAMIVUDINE
02 2AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
03 7AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
04 4ATORVASTATIN CALCIUM; EZETIMIBE
05 2ATROPINE SULFATE; EDROPHONIUM CHLORIDE
06 1AZACITIDINE
07 1CAPREOMYCIN SULFATE
08 2CHLOROTHIAZIDE
09 1CHLOROTHIAZIDE; RESERPINE
10 2CHOLINE FENOFIBRATE
11 1CLINDAMYCIN PHOSPHATE
12 1COSYNTROPIN
13 6DEFERASIROX
14 2DYPHYLLINE
15 1EDROPHONIUM CHLORIDE
16 1EFAVIRENZ
17 1EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
18 2EPROSARTAN MESYLATE
19 3ESTROPIPATE
20 2ETIDRONATE DISODIUM
21 2FENOFIBRATE
22 1FLUVASTATIN SODIUM
23 3FLUVOXAMINE MALEATE
24 3GLIMEPIRIDE
25 1HYDROCHLOROTHIAZIDE
26 2ISRADIPINE
27 2LAMIVUDINE
28 2LAMIVUDINE; ZIDOVUDINE
29 1LETROZOLE
30 1LEVOFLOXACIN
31 2LEVOLEUCOVORIN CALCIUM
32 1MESALAMINE
33 2METFORMIN HYDROCHLORIDE
34 2METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
35 1METHYCLOTHIAZIDE
36 1MONTELUKAST SODIUM
37 1NEVIRAPINE
38 2NIZATIDINE
39 1OXYMETHOLONE
40 1PACLITAXEL
41 1PANTOPRAZOLE SODIUM
42 3PIOGLITAZONE HYDROCHLORIDE
43 8POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
44 2POTASSIUM CHLORIDE
45 2PROMETHAZINE HYDROCHLORIDE
46 5RANITIDINE HYDROCHLORIDE
47 3REPAGLINIDE
48 1RITONAVIR
49 2SELEGILINE HYDROCHLORIDE
50 3SERTRALINE HYDROCHLORIDE
51 6STAVUDINE
52 1SUMATRIPTAN SUCCINATE
53 1TADALAFIL
54 5TENOFOVIR DISOPROXIL FUMARATE
55 1TOLBUTAMIDE
56 2TRIAMCINOLONE ACETONIDE
57 1URSODIOL
58 2ZIDOVUDINE
01 1AEROSOL, FOAM;TOPICAL
02 2CAPSULE, DELAYED RELEASE;ORAL
03 18CAPSULE;ORAL
04 2CREAM;TOPICAL
05 8FOR SOLUTION;ORAL
06 3GRANULE;ORAL
07 6INJECTABLE;INJECTION
08 1INJECTABLE;INTRAVENOUS
09 1INJECTABLE;SUBCUTANEOUS
10 1POWDER;INTRAVENOUS, SUBCUTANEOUS
11 1SOLUTION/DROPS;OPHTHALMIC
12 2SOLUTION;INTRAVENOUS
13 3SUPPOSITORY;RECTAL
14 8TABLET, EXTENDED RELEASE;ORAL
15 1TABLET, FOR SUSPENSION;ORAL
16 66TABLET;ORAL
01 10.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 20.14MG/ML;10MG/ML
04 10.25MG/VIAL
05 10.5%
06 10.5MG
07 10.75MG
08 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 11.25MG;1.25MG;1.25MG;1.25MG
10 11.5MG
11 11.875MG;1.875MG;1.875MG;1.875MG
12 4100MG
13 1100MG/VIAL
14 110MEQ
15 110MG
16 110MG/ML
17 112.5MG
18 112.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 1120GM/PACKET;1.49GM/PACKET;3.36GM/PACKET;2.92GM/PACKET;11.36GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 1130MG
21 3150MG
22 2150MG;300MG
23 115MG
24 2180MG
25 11GM
26 21MG
27 12.5MG
28 12.5MG;2.5MG;2.5MG;2.5MG
29 3200MG
30 1200MG;300MG
31 120MG
32 2227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
33 1227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
34 1240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT
35 2240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
36 2250MG
37 1250MG;0.125MG
38 125MG
39 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
40 22MG
41 13.125MG;3.125MG;3.125MG;3.125MG
42 13.75MG;3.75MG;3.75MG;3.75MG
43 6300MG
44 230MG
45 1360GM/PACKET;4.47GM/PACKET;10.08GM/PACKET;8.76GM/PACKET;34.08GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 2360MG
47 13MG
48 2400MG
49 240MG
50 143MG
51 14MG
52 3500MG
53 1500MG;EQ 15MG BASE
54 250MG
55 35MG
56 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
57 15MG;5MG;5MG;5MG
58 1600MG
59 16MG/ML
60 17.5MG;7.5MG;7.5MG;7.5MG
61 1750MG
62 1850MG;EQ 15MG BASE
63 18MEQ
64 290MG
65 1EQ 100MG BASE
66 1EQ 10MG BASE
67 1EQ 10MG BASE;10MG
68 1EQ 10MG BASE;40MG
69 1EQ 135MG FENOFIBRIC ACID
70 2EQ 150MG BASE
71 1EQ 15MG BASE
72 1EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)
73 1EQ 1GM BASE/VIAL
74 1EQ 20MG BASE;10MG
75 1EQ 250MG BASE/25ML (EQ 10MG BASE/ML)
76 1EQ 25MG BASE
77 2EQ 300MG BASE
78 1EQ 30MG BASE
79 1EQ 400MG BASE
80 1EQ 40MG BASE/VIAL
81 1EQ 40MG BASE;10MG
82 1EQ 45MG BASE
83 1EQ 45MG FENOFIBRIC ACID
84 1EQ 50MG BASE
85 1EQ 5MG BASE;40MG
86 1EQ 600MG BASE
87 1EQ 60MG BASE;30MG
88 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
89 1EQ 75MG BASE
90 1EQ 80MG BASE
91 1EQ 80MG BASE;10MG
01 109DISCN
02 15RX
RLD : Yes
TE Code :
Dosage Form : TABLET, FOR SUSPENSION; ORAL
Proprietary Name : ABACAVIR SULFATE AND LAM...
Dosage Strength : EQ 60MG BASE;30MG
Approval Date : 2023-12-22
Application Number : 204311
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE; ORAL
Proprietary Name : AMLODIPINE BESYLATE AND ...
Dosage Strength : EQ 5MG BASE;40MG
Approval Date : 2011-07-05
Application Number : 79047
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE; ORAL
Proprietary Name : AMLODIPINE BESYLATE AND ...
Dosage Strength : EQ 10MG BASE;40MG
Approval Date : 2011-07-05
Application Number : 79047
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
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 : 2015-11-10
Application Number : 206721
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
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 : 2015-11-10
Application Number : 206721
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
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 : 2015-11-10
Application Number : 206721
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
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 : 2015-11-10
Application Number : 206721
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
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 : 2015-11-10
Application Number : 206721
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
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 : 2015-11-10
Application Number : 206721
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
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 : 2015-11-10
Application Number : 206721
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
