01 3CARBAMAZEPINE
02 2DESVENLAFAXINE
03 1DONEPEZIL HYDROCHLORIDE
04 5HYDROMORPHONE HYDROCHLORIDE
05 12METHYLPHENIDATE HYDROCHLORIDE
06 3NIFEDIPINE
07 1OMEGA-3-ACID ETHYL ESTERS TYPE A
08 3OXYBUTYNIN CHLORIDE
09 4VENLAFAXINE HYDROCHLORIDE
01 1CAPSULE;ORAL
02 32TABLET, EXTENDED RELEASE;ORAL
03 1TABLET;ORAL
01 11.2GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS
02 2100MG
03 110MG
04 112MG
05 115MG
06 116MG
07 218MG
08 1200MG
09 123MG
10 124MG
11 227MG
12 130MG
13 132MG
14 236MG
15 1400MG
16 145MG
17 150MG
18 254MG
19 15MG
20 160MG
21 163MG
22 272MG
23 18MG
24 190MG
25 1EQ 150MG BASE
26 1EQ 225MG BASE
27 1EQ 37.5MG BASE
28 1EQ 75MG BASE
01 4DISCN
02 30RX
RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : CARBAMAZEPINE
Dosage Strength : 100MG
Approval Date : 2024-10-22
Application Number : 215664
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : CARBAMAZEPINE
Dosage Strength : 200MG
Approval Date : 2024-10-22
Application Number : 215664
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : CARBAMAZEPINE
Dosage Strength : 400MG
Approval Date : 2024-10-22
Application Number : 215664
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : KHEDEZLA
Dosage Strength : 50MG
Approval Date : 2013-07-10
Application Number : 204683
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : KHEDEZLA
Dosage Strength : 100MG
Approval Date : 2013-07-10
Application Number : 204683
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DONEPEZIL HYDROCHLORIDE
Dosage Strength : 23MG
Approval Date : 2016-01-26
Application Number : 203114
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : HYDROMORPHONE HYDROCHLOR...
Dosage Strength : 8MG
Approval Date : 2016-07-07
Application Number : 205629
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : HYDROMORPHONE HYDROCHLOR...
Dosage Strength : 12MG
Approval Date : 2016-07-07
Application Number : 205629
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : HYDROMORPHONE HYDROCHLOR...
Dosage Strength : 16MG
Approval Date : 2016-07-07
Application Number : 205629
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : HYDROMORPHONE HYDROCHLOR...
Dosage Strength : 32MG
Approval Date : 2016-07-07
Application Number : 205629
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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