01 1ABACAVIR SULFATE; LAMIVUDINE
02 6AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
03 7AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
04 1ANASTROZOLE
05 6ARIPIPRAZOLE
06 2ATROPINE SULFATE; EDROPHONIUM CHLORIDE
07 1AZACITIDINE
08 2AZELASTINE HYDROCHLORIDE
09 4BUTABARBITAL SODIUM
10 1CAPREOMYCIN SULFATE
11 2CHLOROTHIAZIDE
12 2CHLOROTHIAZIDE; RESERPINE
13 2CHLORPROPAMIDE
14 2CHOLINE FENOFIBRATE
15 3CINACALCET HYDROCHLORIDE
16 1CLINDAMYCIN PHOSPHATE
17 1COSYNTROPIN
18 9DEFERASIROX
19 2DYPHYLLINE
20 1EDROPHONIUM CHLORIDE
21 1EFAVIRENZ
22 1EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
23 2EPROSARTAN MESYLATE
24 3ESCITALOPRAM OXALATE
25 3ESTROPIPATE
26 2ETIDRONATE DISODIUM
27 2FENOFIBRATE
28 1FLUVASTATIN SODIUM
29 3FLUVOXAMINE MALEATE
30 3GLIMEPIRIDE
31 1HYDROCHLOROTHIAZIDE
32 2ISRADIPINE
33 1KETOCONAZOLE
34 2LAMIVUDINE
35 2LAMIVUDINE; ZIDOVUDINE
36 1LETROZOLE
37 1LEVOFLOXACIN
38 2LEVOLEUCOVORIN CALCIUM
39 1MESALAMINE
40 2METFORMIN HYDROCHLORIDE
41 2METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
42 1METHYCLOTHIAZIDE
43 1MONTELUKAST SODIUM
44 2NEVIRAPINE
45 2NIZATIDINE
46 1OXYMETHOLONE
47 1PACLITAXEL
48 1PANTOPRAZOLE SODIUM
49 3PIOGLITAZONE HYDROCHLORIDE
50 8POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
51 2POTASSIUM CHLORIDE
52 2PROMETHAZINE HYDROCHLORIDE
53 5RANITIDINE HYDROCHLORIDE
54 3REPAGLINIDE
55 1RITONAVIR
56 2ROCURONIUM BROMIDE
57 2SELEGILINE HYDROCHLORIDE
58 3SERTRALINE HYDROCHLORIDE
59 6STAVUDINE
60 2SULFANILAMIDE
61 1SUMATRIPTAN SUCCINATE
62 1TADALAFIL
63 5TENOFOVIR DISOPROXIL FUMARATE
64 1TOLBUTAMIDE
65 3TRETINOIN
66 2TRIAMCINOLONE ACETONIDE
67 1URSODIOL
68 5VENLAFAXINE HYDROCHLORIDE
69 2ZIDOVUDINE
01 2AEROSOL, FOAM;TOPICAL
02 2CAPSULE, DELAYED RELEASE;ORAL
03 25CAPSULE;ORAL
04 2CREAM;TOPICAL
05 1CREAM;VAGINAL
06 8FOR SOLUTION;ORAL
07 3GEL;TOPICAL
08 3GRANULE;ORAL
09 8INJECTABLE;INJECTION
10 1INJECTABLE;INTRAVENOUS
11 1INJECTABLE;SUBCUTANEOUS
12 1POWDER;INTRAVENOUS, SUBCUTANEOUS
13 2SOLUTION/DROPS;OPHTHALMIC
14 2SOLUTION;INTRAVENOUS
15 1SPRAY, METERED;NASAL
16 3SUPPOSITORY;RECTAL
17 1SUPPOSITORY;VAGINAL
18 8TABLET, EXTENDED RELEASE;ORAL
19 4TABLET, FOR SUSPENSION;ORAL
20 85TABLET;ORAL
01 10.025%
02 10.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 10.04%
04 10.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 10.1%
06 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 10.137MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 20.14MG/ML;10MG/ML
09 10.25MG/VIAL
10 10.5%
11 10.5MG
12 10.75MG
13 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 11.05GM
15 11.25MG;1.25MG;1.25MG;1.25MG
16 11.5MG
17 11.875MG;1.875MG;1.875MG;1.875MG
18 5100MG
19 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 1100MG/10ML (10MG/ML)
21 1100MG/VIAL
22 110MEQ
23 210MG
24 110MG/ML
25 112.5MG
26 112.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 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**
28 1125MG
29 1130MG
30 115% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 3150MG
32 2150MG;300MG
33 215MG
34 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 2180MG
36 11GM
37 31MG
38 12% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
39 12.5MG
40 12.5MG;2.5MG;2.5MG;2.5MG
41 4200MG
42 1200MG;300MG
43 220MG
44 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**
45 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**
46 1240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT
47 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**
48 4250MG
49 1250MG;0.125MG
50 125MG
51 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
52 32MG
53 13.125MG;3.125MG;3.125MG;3.125MG
54 13.75MG;3.75MG;3.75MG;3.75MG
55 6300MG
56 430MG
57 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**
58 2360MG
59 13MG
60 2400MG
61 240MG
62 143MG
63 14MG
64 4500MG
65 1500MG;0.125MG
66 1500MG;EQ 15MG BASE
67 250MG
68 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
69 150MG/5ML (10MG/ML)
70 45MG
71 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
72 15MG;5MG;5MG;5MG
73 1600MG
74 16MG/ML
75 17.5MG;7.5MG;7.5MG;7.5MG
76 1750MG
77 1850MG;EQ 15MG BASE
78 18MEQ
79 290MG
80 2EQ 100MG BASE
81 2EQ 10MG BASE
82 1EQ 10MG BASE;20MG
83 1EQ 10MG BASE;40MG
84 1EQ 135MG FENOFIBRIC ACID
85 2EQ 150MG BASE
86 1EQ 15MG BASE
87 1EQ 175MG BASE/17.5ML (EQ 10MG BASE/ML)
88 1EQ 1GM BASE/VIAL
89 1EQ 2.5MG BASE;10MG
90 1EQ 20MG BASE
91 1EQ 250MG BASE/25ML (EQ 10MG BASE/ML)
92 2EQ 25MG BASE
93 2EQ 300MG BASE
94 2EQ 30MG BASE
95 1EQ 37.5MG BASE
96 1EQ 400MG BASE
97 1EQ 40MG BASE/VIAL
98 1EQ 45MG BASE
99 1EQ 45MG FENOFIBRIC ACID
100 2EQ 50MG BASE
101 1EQ 5MG BASE
102 1EQ 5MG BASE;10MG
103 1EQ 5MG BASE;20MG
104 1EQ 5MG BASE;40MG
105 1EQ 600MG BASE
106 1EQ 60MG BASE
107 1EQ 60MG BASE;30MG
108 1EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
109 2EQ 75MG BASE
110 1EQ 80MG BASE
111 1EQ 90MG BASE
01 152DISCN
02 11RX
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 2.5MG BASE;10MG
Approval Date : 2010-05-21
Application Number : 77375
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 5MG BASE;10MG
Approval Date : 2010-05-21
Application Number : 77375
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 5MG BASE;20MG
Approval Date : 2010-05-21
Application Number : 77375
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;20MG
Approval Date : 2010-05-21
Application Number : 77375
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 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 :
