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 7BUPRENORPHINE HYDROCHLORIDE
10 4BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
11 1CARBIDOPA
12 1CICLOPIROX
13 1CITALOPRAM HYDROBROMIDE
14 2DAPSONE
15 4DEXAMETHASONE
16 1DISULFIRAM
17 1ECONAZOLE NITRATE
18 1ESTRADIOL
19 1ETHACRYNIC ACID
20 1EXEMESTANE
21 2FELBAMATE
22 4FLECAINIDE ACETATE
23 5FLUOCINONIDE
24 5GABAPENTIN
25 3HYDROCHLOROTHIAZIDE; LISINOPRIL
26 13HYDROCODONE BITARTRATE
27 6IBRUTINIB
28 4LABETALOL HYDROCHLORIDE
29 1LEVONORGESTREL
30 12LEVOTHYROXINE SODIUM
31 7LISDEXAMFETAMINE DIMESYLATE
32 4LORAZEPAM
33 1MELPHALAN
34 1METHENAMINE HIPPURATE
35 9METHYLPHENIDATE HYDROCHLORIDE
36 3MINOCYCLINE HYDROCHLORIDE
37 2NATEGLINIDE
38 2NEVIRAPINE
39 3NIFEDIPINE
40 3NITROFURANTOIN, MACROCRYSTALLINE
41 2NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
42 2OFLOXACIN
43 1OSELTAMIVIR PHOSPHATE
44 3OXYCODONE HYDROCHLORIDE
45 6PREGABALIN
46 1PRIMAQUINE PHOSPHATE
47 1PYRIDOSTIGMINE BROMIDE
48 1PYRIMETHAMINE
49 1RIFAXIMIN
50 3RIVASTIGMINE
51 2SERTRALINE HYDROCHLORIDE
52 1SODIUM PHENYLBUTYRATE
53 1TERIPARATIDE
54 1TOLCAPONE
55 2TRAZODONE HYDROCHLORIDE
56 1VENLAFAXINE BESYLATE
57 1ZOLPIDEM TARTRATE
01 10CAPSULE, EXTENDED RELEASE;ORAL
02 21CAPSULE;ORAL
03 3CREAM;TOPICAL
04 1CREAM;VAGINAL
05 8FILM, EXTENDED RELEASE;TRANSDERMAL
06 7FILM;BUCCAL
07 4FILM;BUCCAL, SUBLINGUAL
08 1FOR SUSPENSION;ORAL
09 2GEL;TOPICAL
10 1OINTMENT;TOPICAL
11 1SOLUTION/DROPS;OPHTHALMIC
12 1SOLUTION/DROPS;OTIC
13 2SOLUTION;INHALATION, ORAL
14 1SOLUTION;SUBCUTANEOUS
15 1SOLUTION;TOPICAL
16 26TABLET, EXTENDED RELEASE;ORAL
17 84TABLET;ORAL
01 10.01%
02 10.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
03 10.05%
04 40.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 10.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
06 10.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
07 10.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
08 10.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
09 10.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
10 10.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
11 10.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
12 10.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
13 10.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
14 10.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
15 20.3%
16 10.3MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
17 10.5MG
18 10.62MG/2.48ML (0.25MG/ML)
19 10.75MG
20 10.77% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 11.25MG;1.25MG;1.25MG;1.25MG
23 21.5MG
24 11.875MG;1.875MG;1.875MG;1.875MG
25 110%
26 6100MG
27 2100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 110MCG/HR
29 410MG
30 112.5MG;10MG
31 112.5MG;20MG
32 2120MG
33 1125MG
34 113.3MG/24HR
35 2140MG
36 1150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
37 115MCG/HR
38 215MG
39 2165MG
40 1180MG
41 118MG
42 11GM
43 11MG
44 12.5MG;2.5MG;2.5MG;2.5MG
45 120%
46 2200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
47 120MCG/HR
48 520MG
49 1250MG
50 625MG
51 125MG;20MG
52 127MG
53 1280MG
54 22MG
55 13.125MG;3.125MG;3.125MG;3.125MG
56 13.75MG;3.75MG;3.75MG;3.75MG
57 1300MG
58 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
59 1300MG;10MG
60 1300MG;50MG
61 1300MG;5MG
62 1300MG;7.5MG
63 430MG
64 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
65 2325MG;10MG
66 1325MG;2.5MG
67 1325MG;50MG
68 1325MG;50MG;40MG
69 2325MG;5MG
70 2325MG;7.5MG
71 2330MG
72 136MG
73 13MG
74 14.6MG/24HR
75 2400MG
76 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
77 340MG
78 1420MG
79 1450MG
80 14MG
81 1500MG
82 450MG
83 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
84 154MG
85 1550MG
86 1560MG
87 15MCG/HR
88 25MG
89 15MG;5MG;5MG;5MG
90 2600MG
91 360MG
92 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
93 162.5MG
94 16MG
95 17.5MCG/HR
96 17.5MG
97 17.5MG;7.5MG;7.5MG;7.5MG
98 270MG
99 1750MG
100 275MG;25MG
101 180MG
102 282.5MG
103 19.5MG/24HR
104 1900MG
105 190MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
106 1EQ 0.075MG BASE
107 1EQ 0.15MG BASE
108 1EQ 0.3MG BASE
109 1EQ 0.45MG BASE
110 1EQ 0.6MG BASE
111 1EQ 0.75MG BASE
112 1EQ 0.9MG BASE
113 1EQ 100MG BASE
114 1EQ 112.5MG BASE
115 1EQ 12MG BASE;EQ 3MG BASE
116 1EQ 150MG BASE
117 1EQ 15MG BASE
118 1EQ 200MG BASE
119 1EQ 2MG BASE;EQ 0.5MG BASE
120 1EQ 30MG BASE
121 1EQ 4MG BASE;EQ 1MG BASE
122 1EQ 50MG BASE
123 1EQ 6MG BASE/ML
124 1EQ 75MG BASE
125 1EQ 8MG BASE;EQ 2MG BASE
01 70DISCN
02 97RX
03 7Blank
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 :
Alvogen is a supplier offers 2 products (APIs, Excipients or Intermediates).
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