01 2ACETYLCYSTEINE
02 1AMLODIPINE BENZOATE
03 3AMLODIPINE BESYLATE; INDAPAMIDE; TELMISARTAN
04 7AMPHETAMINE SULFATE
05 1APREPITANT
06 1ARFORMOTEROL TARTRATE
07 2AZILSARTAN KAMEDOXOMIL
08 2AZILSARTAN KAMEDOXOMIL; CHLORTHALIDONE
09 1BACLOFEN
10 1BENDAMUSTINE HYDROCHLORIDE
11 3CABOZANTINIB
12 1CARMUSTINE
13 1CLONIDINE HYDROCHLORIDE
14 1DEOXYCHOLIC ACID
15 3DEXMEDETOMIDINE HYDROCHLORIDE
16 7DEXTROAMPHETAMINE SULFATE
17 2ENALAPRIL MALEATE
18 5ERYTHROMYCIN
19 6ERYTHROMYCIN ETHYLSUCCINATE
20 3ERYTHROMYCIN STEARATE
21 1ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
22 1FORMOTEROL FUMARATE
23 2GABAPENTIN ENACARBIL
24 1GLYCOPYRROLATE; NEOSTIGMINE METHYLSULFATE
25 1HYDRALAZINE HYDROCHLORIDE; ISOSORBIDE DINITRATE
26 1ICATIBANT ACETATE
27 1IVERMECTIN
28 1LINCOMYCIN HYDROCHLORIDE
29 1LISDEXAMFETAMINE DIMESYLATE
30 1LISINOPRIL
31 4LOMUSTINE
32 1MAGNESIUM SULFATE; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM SULFATE
33 1MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM SULFATE
34 1MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
35 1MELOXICAM
36 1METARAMINOL BITARTRATE
37 1METHOTREXATE SODIUM
38 2METHYLPREDNISOLONE ACETATE
39 1MYCOPHENOLATE MOFETIL
40 2NILOTINIB TARTRATE
41 2NIMODIPINE
42 1OMEGA-3-ACID ETHYL ESTERS
43 1OMEPRAZOLE; SODIUM BICARBONATE
44 4PERPHENAZINE
45 2POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
46 2POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
47 1SITAGLIPTIN HYDROCHLORIDE
48 1SOTALOL HYDROCHLORIDE
49 2TESTOSTERONE CYPIONATE
50 4TIAGABINE HYDROCHLORIDE
51 1TOPIRAMATE
52 1TRIPTORELIN PAMOATE
53 2VANCOMYCIN HYDROCHLORIDE
54 7VERAPAMIL HYDROCHLORIDE
55 1ZONISAMIDE
01 7CAPSULE, EXTENDED RELEASE;ORAL
02 6CAPSULE;ORAL
03 8FOR SOLUTION;ORAL
04 1FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
05 1FOR SUSPENSION;ORAL
06 1IMPLANT;INTRACRANIAL
07 8INJECTABLE;INJECTION
08 1INJECTABLE;INTRAVENOUS
09 1INJECTABLE;SUBCUTANEOUS
10 1LOTION;TOPICAL
11 2SOLUTION;INHALATION
12 1SOLUTION;INTRAMUSCULAR
13 3SOLUTION;INTRAVENOUS
14 11SOLUTION;ORAL
15 1SOLUTION;SUBCUTANEOUS
16 1SOLUTION;TOPICAL
17 8SUSPENSION;ORAL
18 2TABLET, CHEWABLE;ORAL
19 2TABLET, COATED PARTICLES;ORAL
20 2TABLET, DELAYED RELEASE;ORAL
21 2TABLET, EFFERVESCENT;ORAL
22 2TABLET, EXTENDED RELEASE;ORAL
23 5TABLET, ORALLY DISINTEGRATING;ORAL
24 3TABLET; ORAL
25 31TABLET;ORAL
01 10.02MG/2ML
02 10.02MG/ML
03 10.02MG;1MG
04 10.225GM;0.188GM;1.479GM
05 10.5%
06 10.6MG/3ML (0.2MG/ML);3MG/3ML (1MG/ML)
07 10.9GM/BOT;178.7GM/BOT;1.12GM/BOT;0.5GM/BOT;7.3GM/BOT
08 11.6GM/BOT;3.13GM/BOT;17.5GM/BOT
09 2100MG
10 1100MG/4ML (25MG/ML)
11 1100MG/5ML
12 410MG
13 110MG/ML
14 1120MG
15 112MG
16 1130MG/18ML (7.2MG/ML)
17 113MG
18 215MG
19 216MG
20 1180MG
21 11GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS
22 21MG/ML
23 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
24 12%
25 12.5GM
26 12.5MG
27 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 1200MG
29 2200MG/ML
30 1200MG/ML (200MG/ML)
31 220MG
32 120MG/2ML (10MG/ML)
33 1227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET
34 1236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT
35 1240MG
36 1250MG
37 125MG/5ML
38 125MG/ML
39 126MG
40 22MG
41 12MG/ML;84MG/ML
42 2300MG
43 130MG
44 130MG/ML (30MG/ML)
45 2333MG
46 1360MG
47 137.5MG;20MG
48 139MG
49 13MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 140MG
51 140MG/ML
52 2420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
53 24MG
54 2500MG
55 45MG
56 15MG/ML (5MG/ML)
57 1600MG
58 16MG/ML
59 17.5MG
60 17.7MG
61 180MG/ML
62 18MG
63 1EQ 0.015MG BASE/2ML
64 1EQ 1.25MG BASE;0.625MG;10MG
65 1EQ 10MG BASE/ML
66 1EQ 125MG BASE
67 1EQ 1MG BASE/ML
68 1EQ 2.5MG BASE/ML
69 1EQ 2.5MG BASE;1.25MG;20MG
70 1EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)
71 2EQ 200MG BASE
72 1EQ 200MG BASE/5ML
73 1EQ 200MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
74 1EQ 22.5MG BASE/VIAL
75 1EQ 250MG BASE
76 2EQ 25MG BASE/ML
77 1EQ 300MG BASE/ML
78 1EQ 30MG BASE/3ML (EQ 10MG BASE/ML)
79 1EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)
80 1EQ 400MG BASE/5ML
81 1EQ 400MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
82 1EQ 40MG MEDOXOMIL
83 1EQ 40MG MEDOXOMIL;12.5MG
84 1EQ 40MG MEDOXOMIL;25MG
85 1EQ 500MG BASE
86 1EQ 50MG BASE/ML
87 1EQ 5MG BASE;2.5MG;40MG
88 1EQ 71MG BASE
89 1EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)
90 1EQ 80MG MEDOXOMIL
91 1EQ 95MG BASE
01 34DISCN
02 1OTC
03 72RX
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 : 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 : DISCN
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 : DISCN
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 : DISCN
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 :
Azurity Pharma is a supplier offers 1 products (APIs, Excipients or Intermediates).
Find a price of Glucagon bulk offered by Azurity Pharma
