01 2ACETYLCYSTEINE
02 1ACLIDINIUM BROMIDE
03 1ACLIDINIUM BROMIDE; FORMOTEROL FUMARATE
04 1AMLODIPINE BENZOATE
05 3AMLODIPINE BESYLATE; INDAPAMIDE; TELMISARTAN
06 7AMPHETAMINE SULFATE
07 1APREPITANT
08 1ARFORMOTEROL TARTRATE
09 2AZILSARTAN KAMEDOXOMIL
10 2AZILSARTAN KAMEDOXOMIL; CHLORTHALIDONE
11 1BACLOFEN
12 1BENDAMUSTINE HYDROCHLORIDE
13 3CABOZANTINIB
14 1CARMUSTINE
15 2CICLESONIDE
16 1CLONIDINE HYDROCHLORIDE
17 1DEOXYCHOLIC ACID
18 3DEXMEDETOMIDINE HYDROCHLORIDE
19 7DEXTROAMPHETAMINE SULFATE
20 2DIGOXIN
21 2ENALAPRIL MALEATE
22 5ERYTHROMYCIN
23 6ERYTHROMYCIN ETHYLSUCCINATE
24 3ERYTHROMYCIN STEARATE
25 1ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
26 3FERUMOXYTOL
27 1FORMOTEROL FUMARATE
28 2GABAPENTIN ENACARBIL
29 1GLYCOPYRROLATE; NEOSTIGMINE METHYLSULFATE
30 1HYDRALAZINE HYDROCHLORIDE; ISOSORBIDE DINITRATE
31 1ICATIBANT ACETATE
32 1IVERMECTIN
33 1LINCOMYCIN HYDROCHLORIDE
34 1LISDEXAMFETAMINE DIMESYLATE
35 1LISINOPRIL
36 4LOMUSTINE
37 4LOVASTATIN
38 1MAGNESIUM SULFATE; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM SULFATE
39 1MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM SULFATE
40 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
41 1MELOXICAM
42 1METARAMINOL BITARTRATE
43 1METHOTREXATE SODIUM
44 2METHYLPREDNISOLONE ACETATE
45 1MYCOPHENOLATE MOFETIL
46 2NILOTINIB TARTRATE
47 2NIMODIPINE
48 8NISOLDIPINE
49 1OMEGA-3-ACID ETHYL ESTERS
50 2OMEPRAZOLE MAGNESIUM
51 1OMEPRAZOLE; SODIUM BICARBONATE
52 4PERPHENAZINE
53 2POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
54 2POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
55 1RILUZOLE
56 1SITAGLIPTIN HYDROCHLORIDE
57 1SOTALOL HYDROCHLORIDE
58 2TESTOSTERONE CYPIONATE
59 4TIAGABINE HYDROCHLORIDE
60 1TOPIRAMATE
61 1TRIPTORELIN PAMOATE
62 2VANCOMYCIN HYDROCHLORIDE
63 7VERAPAMIL HYDROCHLORIDE
64 1ZONISAMIDE
01 1AEROSOL, METERED;NASAL
02 7CAPSULE, EXTENDED RELEASE;ORAL
03 6CAPSULE;ORAL
04 8FOR SOLUTION;ORAL
05 2FOR SUSPENSION, DELAYED RELEASE;ORAL
06 1FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
07 1FOR SUSPENSION;ORAL
08 1IMPLANT;INTRACRANIAL
09 10INJECTABLE;INJECTION
10 1INJECTABLE;INTRAVENOUS
11 1INJECTABLE;SUBCUTANEOUS
12 1LOTION;TOPICAL
13 2POWDER, METERED;INHALATION
14 2SOLUTION;INHALATION
15 1SOLUTION;INTRAMUSCULAR
16 6SOLUTION;INTRAVENOUS
17 11SOLUTION;ORAL
18 1SOLUTION;SUBCUTANEOUS
19 1SOLUTION;TOPICAL
20 1SPRAY, METERED;NASAL
21 8SUSPENSION;ORAL
22 2TABLET, CHEWABLE;ORAL
23 2TABLET, COATED PARTICLES;ORAL
24 2TABLET, DELAYED RELEASE;ORAL
25 2TABLET, EFFERVESCENT;ORAL
26 14TABLET, EXTENDED RELEASE;ORAL
27 5TABLET, ORALLY DISINTEGRATING;ORAL
28 3TABLET; ORAL
29 32TABLET;ORAL
01 10.02MG/2ML
02 10.02MG/ML
03 10.02MG;1MG
04 10.037MG/INH
05 10.05MG/SPRAY
06 10.1MG/ML
07 10.225GM;0.188GM;1.479GM
08 10.25MG/ML
09 10.4MG/INH
10 10.4MG/INH;0.012MG/INH
11 10.5%
12 10.6MG/3ML (0.2MG/ML);3MG/3ML (1MG/ML)
13 10.9GM/BOT;178.7GM/BOT;1.12GM/BOT;0.5GM/BOT;7.3GM/BOT
14 11.6GM/BOT;3.13GM/BOT;17.5GM/BOT
15 2100MG
16 1100MG/4ML (25MG/ML)
17 1100MG/5ML
18 510MG
19 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 110MG/ML
21 1120MG
22 112MG
23 1130MG/18ML (7.2MG/ML)
24 113MG
25 215MG
26 216MG
27 117MG
28 1180MG
29 11GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS
30 21MG/ML
31 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 12%
33 12.5GM
34 12.5MG
35 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
36 1200MG
37 2200MG/ML
38 1200MG/ML (200MG/ML)
39 320MG
40 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
41 120MG/2ML (10MG/ML)
42 1227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET
43 1236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT
44 1240MG
45 125.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 1250MG
47 125MG/5ML
48 125MG/ML
49 126MG
50 22MG
51 12MG/ML;84MG/ML
52 2300MG
53 130MG
54 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
55 130MG/ML (30MG/ML)
56 2333MG
57 134MG
58 1360MG
59 137.5MG;20MG
60 139MG
61 13MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 240MG
63 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
64 140MG/ML
65 2420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
66 24MG
67 2500MG
68 150MG
69 45MG
70 15MG/ML (5MG/ML)
71 1600MG
72 160MG
73 16MG/ML
74 17.5MG
75 17.7MG
76 18.5MG
77 180MG/ML
78 18MG
79 1EQ 0.015MG BASE/2ML
80 1EQ 1.25MG BASE;0.625MG;10MG
81 1EQ 10MG BASE/ML
82 1EQ 10MG BASE/PACKET
83 1EQ 125MG BASE
84 1EQ 1MG BASE/ML
85 1EQ 2.5MG BASE/ML
86 1EQ 2.5MG BASE/PACKET
87 1EQ 2.5MG BASE;1.25MG;20MG
88 1EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)
89 2EQ 200MG BASE
90 1EQ 200MG BASE/5ML
91 1EQ 200MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
92 1EQ 22.5MG BASE/VIAL
93 1EQ 250MG BASE
94 2EQ 25MG BASE/ML
95 1EQ 300MG BASE/ML
96 1EQ 300MG IRON/10ML (EQ 30MG IRON/ML)
97 1EQ 30MG BASE/3ML (EQ 10MG BASE/ML)
98 1EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)
99 1EQ 400MG BASE/5ML
100 1EQ 400MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
101 1EQ 40MG MEDOXOMIL
102 1EQ 40MG MEDOXOMIL;12.5MG
103 1EQ 40MG MEDOXOMIL;25MG
104 1EQ 500MG BASE
105 1EQ 50MG BASE/ML
106 2EQ 510MG IRON/17ML (EQ 30MG IRON/ML)
107 1EQ 5MG BASE;2.5MG;40MG
108 1EQ 71MG BASE
109 1EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)
110 1EQ 80MG MEDOXOMIL
111 1EQ 95MG BASE
01 42DISCN
02 1OTC
03 88RX
04 4Blank
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 : POWDER, METERED; INHALATION
Proprietary Name : TUDORZA PRESSAIR
Dosage Strength : 0.4MG/INH
Approval Date : 2012-07-23
Application Number : 202450
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
ACLIDINIUM BROMIDE; FORMOTEROL FUMARATE
Dosage Form : POWDER, METERED; INHALATION
Proprietary Name : DUAKLIR PRESSAIR
Dosage Strength : 0.4MG/INH;0.012MG/INH
Approval Date : 2019-03-29
Application Number : 210595
RX/OTC/DISCN : RX
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 : Yes
TE Code :
AMLODIPINE BESYLATE; INDAPAMIDE; TELMISARTAN
Dosage Form : TABLET; ORAL
Proprietary Name : WIDAPLIK
Dosage Strength : EQ 1.25MG BASE;0.625MG;1...
Approval Date : 2025-06-05
Application Number : 219423
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
AMLODIPINE BESYLATE; INDAPAMIDE; TELMISARTAN
Dosage Form : TABLET; ORAL
Proprietary Name : WIDAPLIK
Dosage Strength : EQ 2.5MG BASE;1.25MG;20M...
Approval Date : 2025-06-05
Application Number : 219423
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
AMLODIPINE BESYLATE; INDAPAMIDE; TELMISARTAN
Dosage Form : TABLET; ORAL
Proprietary Name : WIDAPLIK
Dosage Strength : EQ 5MG BASE;2.5MG;40MG
Approval Date : 2025-06-05
Application Number : 219423
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
Azurity Pharma is a supplier offers 1 products (APIs, Excipients or Intermediates).
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