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 3DULOXETINE HYDROCHLORIDE
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 6LENALIDOMIDE
29 1LEVONORGESTREL
30 12LEVOTHYROXINE SODIUM
31 7LISDEXAMFETAMINE DIMESYLATE
32 4LORAZEPAM
33 1MELPHALAN
34 9METHYLPHENIDATE HYDROCHLORIDE
35 3MINOCYCLINE HYDROCHLORIDE
36 2NATEGLINIDE
37 2NEVIRAPINE
38 3NIFEDIPINE
39 3NITROFURANTOIN, MACROCRYSTALLINE
40 2NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
41 2OFLOXACIN
42 1OSELTAMIVIR PHOSPHATE
43 3OXYCODONE HYDROCHLORIDE
44 6PREGABALIN
45 1PRIMAQUINE PHOSPHATE
46 1PYRIDOSTIGMINE BROMIDE
47 1PYRIMETHAMINE
48 2RIFAXIMIN
49 3RIVASTIGMINE
50 2SERTRALINE HYDROCHLORIDE
51 1SODIUM PHENYLBUTYRATE
52 1TERIPARATIDE
53 1TOLCAPONE
54 2TRAZODONE HYDROCHLORIDE
55 1VENLAFAXINE BESYLATE
56 1ZOLPIDEM TARTRATE
01 3CAPSULE, DELAYED REL PELLETS;ORAL
02 10CAPSULE, EXTENDED RELEASE;ORAL
03 28CAPSULE;ORAL
04 3CREAM;TOPICAL
05 3FILM, EXTENDED RELEASE;TRANSDERMAL
06 4FILM;BUCCAL, SUBLINGUAL
07 1FOR SUSPENSION;ORAL
08 2GEL;TOPICAL
09 1OINTMENT;TOPICAL
10 1SOLUTION/DROPS;OPHTHALMIC
11 1SOLUTION/DROPS;OTIC
12 2SOLUTION;INHALATION, ORAL
13 1SOLUTION;SUBCUTANEOUS
14 1SOLUTION;TOPICAL
15 26TABLET, EXTENDED RELEASE;ORAL
16 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02 50.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 510MG
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 315MG
35 2165MG
36 1180MG
37 118MG
38 11MG
39 12.5MG
40 12.5MG;2.5MG;2.5MG;2.5MG
41 120%
42 1200MG
43 2200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
44 620MG
45 1250MG
46 725MG
47 125MG;20MG
48 127MG
49 1280MG
50 22MG
51 13.125MG;3.125MG;3.125MG;3.125MG
52 13.75MG;3.75MG;3.75MG;3.75MG
53 1300MG
54 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
55 1300MG;10MG
56 1300MG;50MG
57 1300MG;5MG
58 1300MG;7.5MG
59 430MG
60 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
61 2325MG;10MG
62 1325MG;2.5MG
63 1325MG;50MG
64 1325MG;50MG;40MG
65 2325MG;5MG
66 2325MG;7.5MG
67 2330MG
68 136MG
69 13MG
70 14.6MG/24HR
71 2400MG
72 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
73 340MG
74 1420MG
75 1450MG
76 14MG
77 1500MG
78 450MG
79 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
80 154MG
81 1550MG
82 1560MG
83 35MG
84 15MG;5MG;5MG;5MG
85 2600MG
86 360MG
87 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
88 162.5MG
89 16MG
90 17.5MG
91 17.5MG;7.5MG;7.5MG;7.5MG
92 270MG
93 1750MG
94 275MG;25MG
95 180MG
96 282.5MG
97 19.5MG/24HR
98 1900MG
99 190MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
100 1EQ 100MG BASE
101 1EQ 112.5MG BASE
102 1EQ 120MG BASE
103 1EQ 12MG BASE;EQ 3MG BASE
104 1EQ 150MG BASE
105 2EQ 15MG BASE
106 1EQ 200MG BASE
107 1EQ 2MG BASE;EQ 0.5MG BASE
108 1EQ 30MG BASE
109 1EQ 4MG BASE;EQ 1MG BASE
110 1EQ 50MG BASE
111 1EQ 6MG BASE/ML
112 1EQ 75MG BASE
113 1EQ 80MG BASE
114 1EQ 8MG BASE;EQ 2MG BASE
115 1EQ 90MG BASE
01 73DISCN
02 90RX
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).
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