01 2ACETYLCYSTEINE
02 1AMLODIPINE BENZOATE
03 7AMPHETAMINE SULFATE
04 1APREPITANT
05 1ARFORMOTEROL TARTRATE
06 2AZILSARTAN KAMEDOXOMIL
07 2AZILSARTAN KAMEDOXOMIL; CHLORTHALIDONE
08 1BACLOFEN
09 1BENDAMUSTINE HYDROCHLORIDE
10 1CARMUSTINE
11 1DEOXYCHOLIC ACID
12 3DEXMEDETOMIDINE HYDROCHLORIDE
13 7DEXTROAMPHETAMINE SULFATE
14 2ENALAPRIL MALEATE
15 11ERYTHROMYCIN
16 12ERYTHROMYCIN ETHYLSUCCINATE
17 3ERYTHROMYCIN STEARATE
18 1ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
19 1FORMOTEROL FUMARATE
20 2GABAPENTIN ENACARBIL
21 1GLYCOPYRROLATE; NEOSTIGMINE METHYLSULFATE
22 1HYDRALAZINE HYDROCHLORIDE; ISOSORBIDE DINITRATE
23 1ICATIBANT ACETATE
24 1IVERMECTIN
25 1LEVOTHYROXINE SODIUM
26 1LISINOPRIL
27 1METARAMINOL BITARTRATE
28 1METHOTREXATE SODIUM
29 2METHYLPREDNISOLONE ACETATE
30 1MYCOPHENOLATE MOFETIL
31 2NIMODIPINE
32 1OMEGA-3-ACID ETHYL ESTERS
33 1OMEPRAZOLE; SODIUM BICARBONATE
34 4PERPHENAZINE
35 1SOTALOL HYDROCHLORIDE
36 2TESTOSTERONE CYPIONATE
37 4TIAGABINE HYDROCHLORIDE
38 1TOPIRAMATE
39 1TRIPTORELIN PAMOATE
40 2VANCOMYCIN HYDROCHLORIDE
41 7VERAPAMIL HYDROCHLORIDE
42 1ZONISAMIDE
01 1CAPSULE, DELAYED REL PELLETS;ORAL
02 7CAPSULE, EXTENDED RELEASE;ORAL
03 2CAPSULE;ORAL
04 3FOR SOLUTION;ORAL
05 1FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
06 1FOR SUSPENSION;ORAL
07 3GRANULE;ORAL
08 1IMPLANT;INTRACRANIAL
09 7INJECTABLE;INJECTION
10 1INJECTABLE;INTRAVENOUS
11 1INJECTABLE;SUBCUTANEOUS
12 1LOTION;TOPICAL
13 2SOLUTION;INHALATION
14 1SOLUTION;INTRAMUSCULAR
15 2SOLUTION;INTRAVENOUS
16 8SOLUTION;ORAL
17 1SOLUTION;SUBCUTANEOUS
18 1SOLUTION;TOPICAL
19 8SUSPENSION;ORAL
20 2TABLET, CHEWABLE;ORAL
21 2TABLET, COATED PARTICLES;ORAL
22 5TABLET, DELAYED RELEASE;ORAL
23 2TABLET, EFFERVESCENT;ORAL
24 2TABLET, EXTENDED RELEASE;ORAL
25 5TABLET, ORALLY DISINTEGRATING;ORAL
26 30TABLET;ORAL
01 10.02MG/2ML
02 10.02MG;1MG
03 10.5%
04 10.6MG/3ML (0.2MG/ML);3MG/3ML (1MG/ML)
05 1100MCG/5ML
06 1100MG
07 1100MG/4ML (25MG/ML)
08 1100MG/5ML
09 310MG
10 1120MG
11 112MG
12 1130MG/18ML (7.2MG/ML)
13 215MG
14 216MG
15 1180MG
16 11GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS
17 21MG/ML
18 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 12%
20 12.5GM
21 12.5MG
22 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 1200MG
24 2200MG/ML
25 1200MG/ML (200MG/ML)
26 220MG
27 120MG/2ML (10MG/ML)
28 1240MG
29 4250MG
30 125MG/5ML
31 125MG/ML
32 22MG
33 12MG/ML;84MG/ML
34 2300MG
35 130MG
36 3333MG
37 1360MG
38 137.5MG;20MG
39 13MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
40 140MG/ML
41 24MG
42 4500MG
43 35MG
44 15MG/ML (5MG/ML)
45 1600MG
46 16MG/ML
47 17.5MG
48 17.7MG
49 180MG/ML
50 18MG
51 1EQ 0.015MG BASE/2ML
52 1EQ 10MG BASE/ML
53 1EQ 125MG BASE
54 1EQ 1MG BASE/ML
55 1EQ 2.5MG BASE/ML
56 1EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)
57 2EQ 200MG BASE
58 3EQ 200MG BASE/5ML
59 1EQ 200MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
60 1EQ 22.5MG BASE/VIAL
61 1EQ 250MG BASE
62 1EQ 25MG BASE/ML
63 1EQ 30MG BASE/3ML (EQ 10MG BASE/ML)
64 1EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)
65 3EQ 400MG BASE
66 2EQ 400MG BASE/5ML
67 1EQ 400MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
68 1EQ 40MG MEDOXOMIL
69 1EQ 40MG MEDOXOMIL;12.5MG
70 1EQ 40MG MEDOXOMIL;25MG
71 1EQ 500MG BASE
72 1EQ 50MG BASE/ML
73 1EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)
74 1EQ 80MG MEDOXOMIL
01 28DISCN
02 1OTC
03 70RX
04 1Blank
RLD : Yes
TE Code :
Dosage Form : TABLET, EFFERVESCENT; ORAL
Proprietary Name : CETYLEV
Dosage Strength : 500MG
Approval Date : 2016-01-29
Application Number : 207916
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, EFFERVESCENT; ORAL
Proprietary Name : CETYLEV
Dosage Strength : 2.5GM
Approval Date : 2016-01-29
Application Number : 207916
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : KATERZIA
Dosage Strength : EQ 1MG BASE/ML
Approval Date : 2019-07-08
Application Number : 211340
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : EVEKEO
Dosage Strength : 5MG
Approval Date : 2012-08-09
Application Number : 200166
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : EVEKEO
Dosage Strength : 10MG
Approval Date : 2012-08-09
Application Number : 200166
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : EVEKEO ODT
Dosage Strength : 5MG
Approval Date : 2019-01-30
Application Number : 209905
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : EVEKEO ODT
Dosage Strength : 10MG
Approval Date : 2019-01-30
Application Number : 209905
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : EVEKEO ODT
Dosage Strength : 15MG
Approval Date : 2019-01-30
Application Number : 209905
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : EVEKEO ODT
Dosage Strength : 20MG
Approval Date : 2019-01-30
Application Number : 209905
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : EVEKEO ODT
Dosage Strength : 2.5MG **Federal Register...
Approval Date : 2021-04-16
Application Number : 209905
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
Azurity Pharma is a supplier offers 1 products (APIs, Excipients or Intermediates).
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