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01 2ACETAMINOPHEN; BUTALBITAL
02 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE
03 7ACETAMINOPHEN; HYDROCODONE BITARTRATE
04 3ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
05 2ACETYLCYSTEINE
06 7AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
07 2BOSENTAN
08 5BUPRENORPHINE
09 4BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
10 1CARBIDOPA
11 1CICLOPIROX
12 1CITALOPRAM HYDROBROMIDE
13 2DAPSONE
14 4DEXAMETHASONE
15 1DISULFIRAM
16 1ECONAZOLE NITRATE
17 1ETHACRYNIC ACID
18 1EXEMESTANE
19 2FELBAMATE
20 4FLECAINIDE ACETATE
21 5FLUOCINONIDE
22 5GABAPENTIN
23 3HYDROCHLOROTHIAZIDE; LISINOPRIL
24 13HYDROCODONE BITARTRATE
25 6IBRUTINIB
26 4LABETALOL HYDROCHLORIDE
27 1LEVONORGESTREL
28 12LEVOTHYROXINE SODIUM
29 7LISDEXAMFETAMINE DIMESYLATE
30 4LORAZEPAM
31 1MELPHALAN
32 1METHENAMINE HIPPURATE
33 9METHYLPHENIDATE HYDROCHLORIDE
34 3MINOCYCLINE HYDROCHLORIDE
35 2NATEGLINIDE
36 2NEVIRAPINE
37 3NIFEDIPINE
38 3NITROFURANTOIN, MACROCRYSTALLINE
39 2NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
40 2OFLOXACIN
41 1OSELTAMIVIR PHOSPHATE
42 3OXYCODONE HYDROCHLORIDE
43 6PREGABALIN
44 1PRIMAQUINE PHOSPHATE
45 1PYRIDOSTIGMINE BROMIDE
46 1PYRIMETHAMINE
47 2RIFAXIMIN
48 3RIVASTIGMINE
49 2SERTRALINE HYDROCHLORIDE
50 1SODIUM PHENYLBUTYRATE
51 1TERIPARATIDE
52 1TOLCAPONE
53 2TRAZODONE HYDROCHLORIDE
54 1VENLAFAXINE BESYLATE
55 1ZOLPIDEM TARTRATE
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01 10CAPSULE, EXTENDED RELEASE;ORAL
02 21CAPSULE;ORAL
03 3CREAM;TOPICAL
04 8FILM, EXTENDED RELEASE;TRANSDERMAL
05 4FILM;BUCCAL, SUBLINGUAL
06 1FOR SUSPENSION;ORAL
07 2GEL;TOPICAL
08 1OINTMENT;TOPICAL
09 1SOLUTION/DROPS;OPHTHALMIC
10 1SOLUTION/DROPS;OTIC
11 2SOLUTION;INHALATION, ORAL
12 1SOLUTION;SUBCUTANEOUS
13 1SOLUTION;TOPICAL
14 26TABLET, EXTENDED RELEASE;ORAL
15 85TABLET;ORAL
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01 10.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
02 50.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 10.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
04 10.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
05 10.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
06 10.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
07 10.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
08 10.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
09 10.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
10 10.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
11 10.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
12 10.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
13 20.3%
14 10.3MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
15 10.56MG/2.24ML (0.25MG/ML)
16 10.5MG
17 10.75MG
18 10.77% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 11.25MG;1.25MG;1.25MG;1.25MG
21 21.5MG
22 11.875MG;1.875MG;1.875MG;1.875MG
23 110%
24 6100MG
25 2100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 110MCG/HR
27 410MG
28 112.5MG;10MG
29 112.5MG;20MG
30 2120MG
31 1125MG
32 113.3MG/24HR
33 2140MG
34 1150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 115MCG/HR
36 215MG
37 2165MG
38 1180MG
39 118MG
40 11GM
41 11MG
42 12.5MG;2.5MG;2.5MG;2.5MG
43 120%
44 1200MG
45 2200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 120MCG/HR
47 520MG
48 1250MG
49 625MG
50 125MG;20MG
51 127MG
52 1280MG
53 22MG
54 13.125MG;3.125MG;3.125MG;3.125MG
55 13.75MG;3.75MG;3.75MG;3.75MG
56 1300MG
57 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
58 1300MG;10MG
59 1300MG;50MG
60 1300MG;5MG
61 1300MG;7.5MG
62 430MG
63 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
64 2325MG;10MG
65 1325MG;2.5MG
66 1325MG;50MG
67 1325MG;50MG;40MG
68 2325MG;5MG
69 2325MG;7.5MG
70 2330MG
71 136MG
72 13MG
73 14.6MG/24HR
74 2400MG
75 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
76 340MG
77 1420MG
78 1450MG
79 14MG
80 1500MG
81 450MG
82 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
83 154MG
84 1550MG
85 1560MG
86 15MCG/HR
87 25MG
88 15MG;5MG;5MG;5MG
89 2600MG
90 360MG
91 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
92 162.5MG
93 16MG
94 17.5MCG/HR
95 17.5MG
96 17.5MG;7.5MG;7.5MG;7.5MG
97 270MG
98 1750MG
99 275MG;25MG
100 180MG
101 282.5MG
102 19.5MG/24HR
103 1900MG
104 190MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
105 1EQ 100MG BASE
106 1EQ 112.5MG BASE
107 1EQ 12MG BASE;EQ 3MG BASE
108 1EQ 150MG BASE
109 1EQ 15MG BASE
110 1EQ 200MG BASE
111 1EQ 2MG BASE;EQ 0.5MG BASE
112 1EQ 30MG BASE
113 1EQ 4MG BASE;EQ 1MG BASE
114 1EQ 50MG BASE
115 1EQ 6MG BASE/ML
116 1EQ 75MG BASE
117 1EQ 8MG BASE;EQ 2MG BASE
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01 67DISCN
02 92RX
03 8Blank
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL AND ACETAMINO...
Dosage Strength : 325MG;50MG
Approval Date : 2015-10-30
Application Number : 205120
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL AND ACETAMINO...
Dosage Strength : 300MG;50MG
Approval Date : 2017-06-05
Application Number : 207635
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL, ACETAMINOPHE...
Dosage Strength : 325MG;50MG;40MG
Approval Date : 2017-01-10
Application Number : 204984
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 300MG;5MG
Approval Date : 2018-11-08
Application Number : 208540
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 300MG;7.5MG
Approval Date : 2018-11-08
Application Number : 208540
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 300MG;10MG
Approval Date : 2018-11-08
Application Number : 208540
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 325MG;2.5MG
Approval Date : 2018-10-24
Application Number : 209958
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 325MG;5MG
Approval Date : 2018-10-24
Application Number : 209958
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 325MG;7.5MG
Approval Date : 2018-10-24
Application Number : 209958
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : HYDROCODONE BITARTRATE A...
Dosage Strength : 325MG;10MG
Approval Date : 2018-10-24
Application Number : 209958
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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