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 1ESCITALOPRAM OXALATE
18 1ETHACRYNIC ACID
19 1EXEMESTANE
20 2FELBAMATE
21 4FLECAINIDE ACETATE
22 5FLUOCINONIDE
23 5GABAPENTIN
24 3HYDROCHLOROTHIAZIDE; LISINOPRIL
25 13HYDROCODONE BITARTRATE
26 6IBRUTINIB
27 4LABETALOL HYDROCHLORIDE
28 1LEVONORGESTREL
29 12LEVOTHYROXINE SODIUM
30 7LISDEXAMFETAMINE DIMESYLATE
31 4LORAZEPAM
32 1MELPHALAN
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
01 10CAPSULE, EXTENDED RELEASE;ORAL
02 22CAPSULE;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 84TABLET;ORAL
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02 50.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 11MG
41 12.5MG;2.5MG;2.5MG;2.5MG
42 120%
43 1200MG
44 2200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
45 120MCG/HR
46 520MG
47 1250MG
48 625MG
49 125MG;20MG
50 127MG
51 1280MG
52 22MG
53 13.125MG;3.125MG;3.125MG;3.125MG
54 13.75MG;3.75MG;3.75MG;3.75MG
55 1300MG
56 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
57 1300MG;10MG
58 1300MG;50MG
59 1300MG;5MG
60 1300MG;7.5MG
61 430MG
62 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
63 2325MG;10MG
64 1325MG;2.5MG
65 1325MG;50MG
66 1325MG;50MG;40MG
67 2325MG;5MG
68 2325MG;7.5MG
69 2330MG
70 136MG
71 13MG
72 14.6MG/24HR
73 2400MG
74 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
75 340MG
76 1420MG
77 1450MG
78 14MG
79 1500MG
80 450MG
81 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
82 154MG
83 1550MG
84 1560MG
85 15MCG/HR
86 25MG
87 15MG;5MG;5MG;5MG
88 2600MG
89 360MG
90 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
91 162.5MG
92 16MG
93 17.5MCG/HR
94 17.5MG
95 17.5MG;7.5MG;7.5MG;7.5MG
96 270MG
97 1750MG
98 275MG;25MG
99 180MG
100 282.5MG
101 19.5MG/24HR
102 1900MG
103 190MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
104 1EQ 100MG BASE
105 1EQ 112.5MG BASE
106 1EQ 12MG BASE;EQ 3MG BASE
107 1EQ 150MG BASE
108 2EQ 15MG BASE
109 1EQ 200MG BASE
110 1EQ 2MG BASE;EQ 0.5MG BASE
111 1EQ 30MG BASE
112 1EQ 4MG BASE;EQ 1MG BASE
113 1EQ 50MG BASE
114 1EQ 6MG BASE/ML
115 1EQ 75MG BASE
116 1EQ 8MG BASE;EQ 2MG BASE
01 74DISCN
02 85RX
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 :
Alvogen is a supplier offers 2 products (APIs, Excipients or Intermediates).
Find a price of Furaltadone HCl bulk offered by Alvogen
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