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 8NISOLDIPINE
43 1OMEGA-3-ACID ETHYL ESTERS
44 2OMEPRAZOLE MAGNESIUM
45 1OMEPRAZOLE; SODIUM BICARBONATE
46 4PERPHENAZINE
47 2POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
48 2POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
49 1SITAGLIPTIN HYDROCHLORIDE
50 1SOTALOL HYDROCHLORIDE
51 2TESTOSTERONE CYPIONATE
52 4TIAGABINE HYDROCHLORIDE
53 1TOPIRAMATE
54 1TRIPTORELIN PAMOATE
55 2VANCOMYCIN HYDROCHLORIDE
56 7VERAPAMIL HYDROCHLORIDE
57 1ZONISAMIDE
01 3ARBOR PHARMS INC
02 7ARBOR PHARMS LLC
03 90AZURITY
04 1SLAYBACK
05 20WILSHIRE PHARMS INC
01 7CAPSULE, EXTENDED RELEASE;ORAL
02 6CAPSULE;ORAL
03 8FOR SOLUTION;ORAL
04 2FOR SUSPENSION, DELAYED RELEASE;ORAL
05 1FOR SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
06 1FOR SUSPENSION;ORAL
07 1IMPLANT;INTRACRANIAL
08 8INJECTABLE;INJECTION
09 1INJECTABLE;INTRAVENOUS
10 1INJECTABLE;SUBCUTANEOUS
11 1LOTION;TOPICAL
12 2SOLUTION;INHALATION
13 1SOLUTION;INTRAMUSCULAR
14 3SOLUTION;INTRAVENOUS
15 11SOLUTION;ORAL
16 1SOLUTION;SUBCUTANEOUS
17 1SOLUTION;TOPICAL
18 8SUSPENSION;ORAL
19 2TABLET, CHEWABLE;ORAL
20 2TABLET, COATED PARTICLES;ORAL
21 2TABLET, DELAYED RELEASE;ORAL
22 2TABLET, EFFERVESCENT;ORAL
23 10TABLET, EXTENDED RELEASE;ORAL
24 5TABLET, ORALLY DISINTEGRATING;ORAL
25 3TABLET; ORAL
26 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 **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 110MG/ML
15 1120MG
16 112MG
17 1130MG/18ML (7.2MG/ML)
18 113MG
19 215MG
20 216MG
21 117MG
22 1180MG
23 11GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS
24 21MG/ML
25 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 12%
27 12.5GM
28 12.5MG
29 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 1200MG
31 2200MG/ML
32 1200MG/ML (200MG/ML)
33 220MG
34 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
35 120MG/2ML (10MG/ML)
36 1227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET
37 1236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT
38 1240MG
39 125.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
40 1250MG
41 125MG/5ML
42 125MG/ML
43 126MG
44 22MG
45 12MG/ML;84MG/ML
46 2300MG
47 130MG
48 130MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
49 130MG/ML (30MG/ML)
50 2333MG
51 134MG
52 1360MG
53 137.5MG;20MG
54 139MG
55 13MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
56 140MG
57 140MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
58 140MG/ML
59 2420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
60 24MG
61 2500MG
62 45MG
63 15MG/ML (5MG/ML)
64 1600MG
65 16MG/ML
66 17.5MG
67 17.7MG
68 18.5MG
69 180MG/ML
70 18MG
71 1EQ 0.015MG BASE/2ML
72 1EQ 1.25MG BASE;0.625MG;10MG
73 1EQ 10MG BASE/ML
74 1EQ 10MG BASE/PACKET
75 1EQ 125MG BASE
76 1EQ 1MG BASE/ML
77 1EQ 2.5MG BASE/ML
78 1EQ 2.5MG BASE/PACKET
79 1EQ 2.5MG BASE;1.25MG;20MG
80 1EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)
81 2EQ 200MG BASE
82 1EQ 200MG BASE/5ML
83 1EQ 200MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
84 1EQ 22.5MG BASE/VIAL
85 1EQ 250MG BASE
86 2EQ 25MG BASE/ML
87 1EQ 300MG BASE/ML
88 1EQ 30MG BASE/3ML (EQ 10MG BASE/ML)
89 1EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)
90 1EQ 400MG BASE/5ML
91 1EQ 400MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
92 1EQ 40MG MEDOXOMIL
93 1EQ 40MG MEDOXOMIL;12.5MG
94 1EQ 40MG MEDOXOMIL;25MG
95 1EQ 500MG BASE
96 1EQ 50MG BASE/ML
97 1EQ 5MG BASE;2.5MG;40MG
98 1EQ 71MG BASE
99 1EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)
100 1EQ 80MG MEDOXOMIL
101 1EQ 95MG BASE
01 121USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, EFFERVESCENT;ORA...
Brand Name : CETYLEV
Dosage Strength : 500MG
Packaging :
Approval Date : 2016-01-29
Application Number : 207916
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, EFFERVESCENT;ORA...
Brand Name : CETYLEV
Dosage Strength : 2.5GM
Packaging :
Approval Date : 2016-01-29
Application Number : 207916
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SUSPENSION;ORAL
Brand Name : KATERZIA
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2019-07-08
Application Number : 211340
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Amlodipine Besylate; Indapamide; Telmisartan
Dosage Form : TABLET;ORAL
Brand Name : WIDAPLIK
Dosage Strength : EQ 1.25MG BASE;0.625MG...
Packaging :
Approval Date : 2025-06-05
Application Number : 219423
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Amlodipine Besylate; Indapamide; Telmisartan
Dosage Form : TABLET;ORAL
Brand Name : WIDAPLIK
Dosage Strength : EQ 2.5MG BASE;1.25MG;2...
Packaging :
Approval Date : 2025-06-05
Application Number : 219423
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Amlodipine Besylate; Indapamide; Telmisartan
Dosage Form : TABLET;ORAL
Brand Name : WIDAPLIK
Dosage Strength : EQ 5MG BASE;2.5MG;40MG
Packaging :
Approval Date : 2025-06-05
Application Number : 219423
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : EVEKEO
Dosage Strength : 5MG
Packaging :
Approval Date : 2012-08-09
Application Number : 200166
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : EVEKEO
Dosage Strength : 10MG
Packaging :
Approval Date : 2012-08-09
Application Number : 200166
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : EVEKEO ODT
Dosage Strength : 5MG
Packaging :
Approval Date : 2019-01-30
Application Number : 209905
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : EVEKEO ODT
Dosage Strength : 10MG
Packaging :
Approval Date : 2019-01-30
Application Number : 209905
Regulatory Info : DISCN
Registration Country : USA
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Find a price of Glucagon bulk offered by Azurity Pharma
