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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 4BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
09 1CARBIDOPA
10 1CICLOPIROX
11 1CITALOPRAM HYDROBROMIDE
12 2DAPSONE
13 4DEXAMETHASONE
14 1DISULFIRAM
15 1ECONAZOLE NITRATE
16 1ESCITALOPRAM OXALATE
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 9METHYLPHENIDATE HYDROCHLORIDE
33 3MINOCYCLINE HYDROCHLORIDE
34 2NATEGLINIDE
35 2NEVIRAPINE
36 3NIFEDIPINE
37 3NITROFURANTOIN, MACROCRYSTALLINE
38 2NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
39 2OFLOXACIN
40 1OSELTAMIVIR PHOSPHATE
41 3OXYCODONE HYDROCHLORIDE
42 6PREGABALIN
43 1PRIMAQUINE PHOSPHATE
44 1PYRIDOSTIGMINE BROMIDE
45 1PYRIMETHAMINE
46 2RIFAXIMIN
47 3RIVASTIGMINE
48 2SERTRALINE HYDROCHLORIDE
49 1SODIUM PHENYLBUTYRATE
50 1TERIPARATIDE
51 1TOLCAPONE
52 2TRAZODONE HYDROCHLORIDE
53 1VENLAFAXINE BESYLATE
54 1ZOLPIDEM TARTRATE
									
									
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01 10CAPSULE, EXTENDED RELEASE;ORAL
02 22CAPSULE;ORAL
03 3CREAM;TOPICAL
04 3FILM, 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
									
									
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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02 50.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 410MG
27 112.5MG;10MG
28 112.5MG;20MG
29 2120MG
30 1125MG
31 113.3MG/24HR
32 2140MG
33 1150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
34 215MG
35 2165MG
36 1180MG
37 118MG
38 11MG
39 12.5MG;2.5MG;2.5MG;2.5MG
40 120%
41 1200MG
42 2200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
43 520MG
44 1250MG
45 625MG
46 125MG;20MG
47 127MG
48 1280MG
49 22MG
50 13.125MG;3.125MG;3.125MG;3.125MG
51 13.75MG;3.75MG;3.75MG;3.75MG
52 1300MG
53 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
54 1300MG;10MG
55 1300MG;50MG
56 1300MG;5MG
57 1300MG;7.5MG
58 430MG
59 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
60 2325MG;10MG
61 1325MG;2.5MG
62 1325MG;50MG
63 1325MG;50MG;40MG
64 2325MG;5MG
65 2325MG;7.5MG
66 2330MG
67 136MG
68 13MG
69 14.6MG/24HR
70 2400MG
71 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
72 340MG
73 1420MG
74 1450MG
75 14MG
76 1500MG
77 450MG
78 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
79 154MG
80 1550MG
81 1560MG
82 25MG
83 15MG;5MG;5MG;5MG
84 2600MG
85 360MG
86 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
87 162.5MG
88 16MG
89 17.5MG
90 17.5MG;7.5MG;7.5MG;7.5MG
91 270MG
92 1750MG
93 275MG;25MG
94 180MG
95 282.5MG
96 19.5MG/24HR
97 1900MG
98 190MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
99 1EQ 100MG BASE
100 1EQ 112.5MG BASE
101 1EQ 12MG BASE;EQ 3MG BASE
102 1EQ 150MG BASE
103 2EQ 15MG BASE
104 1EQ 200MG BASE
105 1EQ 2MG BASE;EQ 0.5MG BASE
106 1EQ 30MG BASE
107 1EQ 4MG BASE;EQ 1MG BASE
108 1EQ 50MG BASE
109 1EQ 6MG BASE/ML
110 1EQ 75MG BASE
111 1EQ 8MG BASE;EQ 2MG BASE
									
									
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01 73DISCN
02 81RX
03 8Blank
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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 :

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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 :

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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 :

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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 :

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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 :

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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 :

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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 :

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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 :

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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 :

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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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