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 2Febuxostat
23 5GABAPENTIN
24 1Glatiramer Acetate
25 3HYDROCHLOROTHIAZIDE; LISINOPRIL
26 13HYDROCODONE BITARTRATE
27 6IBRUTINIB
28 1Klopidogrelbesilat
29 4LABETALOL HYDROCHLORIDE
30 6LENALIDOMIDE
31 1LEVONORGESTREL
32 12LEVOTHYROXINE SODIUM
33 7LISDEXAMFETAMINE DIMESYLATE
34 4LORAZEPAM
35 1MELPHALAN
36 9METHYLPHENIDATE HYDROCHLORIDE
37 3MINOCYCLINE HYDROCHLORIDE
38 2NATEGLINIDE
39 2NEVIRAPINE
40 3NIFEDIPINE
41 3NITROFURANTOIN, MACROCRYSTALLINE
42 2NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
43 2OFLOXACIN
44 1OSELTAMIVIR PHOSPHATE
45 3OXYCODONE HYDROCHLORIDE
46 6PREGABALIN
47 1PRIMAQUINE PHOSPHATE
48 1PYRIDOSTIGMINE BROMIDE
49 1PYRIMETHAMINE
50 2RIFAXIMIN
51 3RIVASTIGMINE
52 2SERTRALINE HYDROCHLORIDE
53 1SODIUM PHENYLBUTYRATE
54 1TERIPARATIDE
55 1TOLCAPONE
56 2TRAZODONE HYDROCHLORIDE
57 1Tamsulosin Hydrochloride; Dutasteride
58 1VENLAFAXINE BESYLATE
59 1ZOLPIDEM TARTRATE
01 22ALMATICA
02 126ALVOGEN
03 2ALVOGEN INC
04 6ALVOGEN PINE BROOK
05 1Alvogen
06 2Alvogen Malta Operations (ROW) Ltd
07 1Alvogen Malta Operations (Row) Limited
08 1Labormed-Pharma Sa
09 11NORWICH
10 1NORWICH PHARMACEUTICALS INC
01 10CAPSULE, EXTENDED RELEASE;ORAL
02 28CAPSULE;ORAL
03 3CREAM;TOPICAL
04 3FILM, EXTENDED RELEASE;TRANSDERMAL
05 4FILM;BUCCAL, SUBLINGUAL
06 1FOR SUSPENSION;ORAL
07 3Film Coated Tablet
08 2GEL;TOPICAL
09 1Hard Capsule
10 1OINTMENT;TOPICAL
11 1Prefilled Syringe
12 1SOLUTION/DROPS;OPHTHALMIC
13 1SOLUTION/DROPS;OTIC
14 2SOLUTION;INHALATION, ORAL
15 1SOLUTION;SUBCUTANEOUS
16 1SOLUTION;TOPICAL
17 26TABLET, EXTENDED RELEASE;ORAL
18 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02 50.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 10.5MG; 0.4 MG
18 10.75MG
19 10.77% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 11.25MG;1.25MG;1.25MG;1.25MG
22 21.5MG
23 11.875MG;1.875MG;1.875MG;1.875MG
24 110%
25 6100MG
26 2100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 510MG
28 112.5MG;10MG
29 112.5MG;20MG
30 3120MG
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 315MG
36 2165MG
37 1180MG
38 118MG
39 11MG
40 12.5MG
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 720MG
46 1250MG
47 725MG
48 125MG;20MG
49 127MG
50 1280MG
51 22MG
52 13.125MG;3.125MG;3.125MG;3.125MG
53 13.75MG;3.75MG;3.75MG;3.75MG
54 1300MG
55 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
56 1300MG;10MG
57 1300MG;50MG
58 1300MG;5MG
59 1300MG;7.5MG
60 430MG
61 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 2325MG;10MG
63 1325MG;2.5MG
64 1325MG;50MG
65 1325MG;50MG;40MG
66 2325MG;5MG
67 2325MG;7.5MG
68 2330MG
69 136MG
70 13MG
71 14.6MG/24HR
72 2400MG
73 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
74 340MG
75 1420MG
76 1450MG
77 14MG
78 1500MG
79 450MG
80 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
81 154MG
82 1550MG
83 1560MG
84 35MG
85 15MG;5MG;5MG;5MG
86 2600MG
87 360MG
88 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
89 162.5MG
90 16MG
91 17.5MG
92 17.5MG;7.5MG;7.5MG;7.5MG
93 270MG
94 1750MG
95 275MG;25MG
96 175mg
97 280MG
98 282.5MG
99 19.5MG/24HR
100 1900MG
101 190MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
102 1EQ 100MG BASE
103 1EQ 112.5MG BASE
104 1EQ 12MG BASE;EQ 3MG BASE
105 1EQ 150MG BASE
106 2EQ 15MG BASE
107 1EQ 200MG BASE
108 1EQ 2MG BASE;EQ 0.5MG BASE
109 1EQ 30MG BASE
110 1EQ 4MG BASE;EQ 1MG BASE
111 1EQ 50MG BASE
112 1EQ 6MG BASE/ML
113 1EQ 75MG BASE
114 1EQ 8MG BASE;EQ 2MG BASE
01 2Malta
02 1Spain
03 1Sweden
04 1U.S.A
05 168USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUTALBITAL AND ACETAMINOP...
Dosage Strength : 325MG;50MG
Packaging :
Approval Date : 2015-10-30
Application Number : 205120
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUTALBITAL AND ACETAMINOP...
Dosage Strength : 300MG;50MG
Packaging :
Approval Date : 2017-06-05
Application Number : 207635
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : TABLET;ORAL
Brand Name : BUTALBITAL, ACETAMINOPHEN...
Dosage Strength : 325MG;50MG;40MG
Packaging :
Approval Date : 2017-01-10
Application Number : 204984
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 300MG;5MG
Packaging :
Approval Date : 2018-11-08
Application Number : 208540
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 300MG;7.5MG
Packaging :
Approval Date : 2018-11-08
Application Number : 208540
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 300MG;10MG
Packaging :
Approval Date : 2018-11-08
Application Number : 208540
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 325MG;2.5MG
Packaging :
Approval Date : 2018-10-24
Application Number : 209958
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 325MG;5MG
Packaging :
Approval Date : 2018-10-24
Application Number : 209958
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 325MG;7.5MG
Packaging :
Approval Date : 2018-10-24
Application Number : 209958
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 325MG;10MG
Packaging :
Approval Date : 2018-10-24
Application Number : 209958
Regulatory Info : DISCN
Registration Country : USA
Alvogen is a supplier offers 2 products (APIs, Excipients or Intermediates).
Find a price of Furaltadone HCl bulk offered by Alvogen
Find a price of Mesalazine bulk offered by Alvogen
