01 3AMLODIPINE BESYLATE
02 8ARIPIPRAZOLE
03 4CETIRIZINE HYDROCHLORIDE
04 1DESLORATADINE
05 3DIVALPROEX SODIUM
06 3ESZOPICLONE
07 3FELODIPINE
08 1GEMIFLOXACIN MESYLATE
09 1GRANISETRON HYDROCHLORIDE
10 1IBANDRONATE SODIUM
11 4LEVETIRACETAM
12 3LEVOFLOXACIN
13 2MEMANTINE HYDROCHLORIDE
14 2MODAFINIL
15 2NARATRIPTAN HYDROCHLORIDE
16 10OLANZAPINE
17 2PANTOPRAZOLE SODIUM
18 2RASAGILINE MESYLATE
19 2RISEDRONATE SODIUM
20 4RIVASTIGMINE TARTRATE
21 7ROPINIROLE HYDROCHLORIDE
22 3SUMATRIPTAN SUCCINATE
23 1TERBINAFINE HYDROCHLORIDE
24 3VENLAFAXINE HYDROCHLORIDE
25 2ZALEPLON
26 2ZOLMITRIPTAN
01 3CAPSULE, EXTENDED RELEASE;ORAL
02 6CAPSULE;ORAL
03 5TABLET, DELAYED RELEASE;ORAL
04 3TABLET, EXTENDED RELEASE;ORAL
05 6TABLET, ORALLY DISINTEGRATING;ORAL
06 56TABLET;ORAL
01 1100MG
02 910MG
03 415MG
04 11GM
05 11MG
06 32.5MG
07 1200MG
08 320MG
09 2250MG
10 22MG
11 230MG
12 135MG
13 13MG
14 2500MG
15 105MG
16 17.5MG
17 2750MG
18 1EQ 0.25MG BASE
19 2EQ 0.5MG BASE
20 1EQ 1.5MG BASE
21 1EQ 100MG BASE
22 1EQ 10MG BASE
23 1EQ 125MG VALPROIC ACID
24 2EQ 150MG BASE
25 4EQ 1MG BASE
26 2EQ 2.5MG BASE
27 1EQ 20MG BASE
28 1EQ 250MG BASE
29 1EQ 250MG VALPROIC ACID
30 1EQ 25MG BASE
31 1EQ 2MG BASE
32 1EQ 320MG BASE
33 1EQ 37.5MG BASE
34 2EQ 3MG BASE
35 1EQ 4.5MG BASE
36 1EQ 40MG BASE
37 1EQ 4MG BASE
38 1EQ 500MG VALPROIC ACID
39 1EQ 50MG BASE
40 2EQ 5MG BASE
41 1EQ 6MG BASE
42 1EQ 75MG BASE
01 3DISCN
02 4OTC
03 72RX
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 2.5MG BASE
Approval Date : 2009-07-02
Application Number : 78453
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 5MG BASE
Approval Date : 2009-07-02
Application Number : 78453
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMLODIPINE BESYLATE
Dosage Strength : EQ 10MG BASE
Approval Date : 2009-07-02
Application Number : 78453
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : ARIPIPRAZOLE
Dosage Strength : 10MG
Approval Date : 2017-12-11
Application Number : 202547
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, ORALLY DISINTEGRATING;...
Proprietary Name : ARIPIPRAZOLE
Dosage Strength : 15MG
Approval Date : 2017-12-11
Application Number : 202547
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ARIPIPRAZOLE
Dosage Strength : 2MG
Approval Date : 2017-05-23
Application Number : 202683
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ARIPIPRAZOLE
Dosage Strength : 5MG
Approval Date : 2017-05-23
Application Number : 202683
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ARIPIPRAZOLE
Dosage Strength : 10MG
Approval Date : 2017-05-23
Application Number : 202683
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ARIPIPRAZOLE
Dosage Strength : 15MG
Approval Date : 2017-05-23
Application Number : 202683
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ARIPIPRAZOLE
Dosage Strength : 20MG
Approval Date : 2017-05-23
Application Number : 202683
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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