01 1ACETAMINOPHEN
02 1ACETAMINOPHEN; IBUPROFEN
03 4CETIRIZINE HYDROCHLORIDE
04 3DULOXETINE HYDROCHLORIDE
05 1ESOMEPRAZOLE MAGNESIUM
06 2FAMOTIDINE
07 3FLUOXETINE HYDROCHLORIDE
08 3GABAPENTIN
09 2GUAIFENESIN
10 6IBUPROFEN
11 2LORATADINE
12 5METFORMIN HYDROCHLORIDE
13 1NAPROXEN SODIUM
14 3PARICALCITOL
01 3CAPSULE, DELAYED REL PELLETS;ORAL
02 1CAPSULE, DELAYED RELEASE;ORAL
03 11CAPSULE;ORAL
04 5TABLET, EXTENDED RELEASE;ORAL
05 17TABLET;ORAL
01 11.2GM
02 1100MG
03 510MG
04 11GM
05 11MCG
06 2200MG
07 120MG
08 1220MG
09 1250MG;125MG
10 12MCG
11 1300MG
12 2400MG
13 14MCG
14 2500MG
15 25MG
16 2600MG
17 1650MG
18 1750MG
19 1800MG
20 1850MG
21 1EQ 10MG BASE
22 1EQ 200MG FREE ACID AND POTASSIUM SALT
23 3EQ 20MG BASE
24 1EQ 30MG BASE
25 1EQ 40MG BASE
26 1EQ 60MG BASE
01 3DISCN
02 16OTC
03 17RX
04 1Blank
RLD : No
TE Code :
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : ACETAMINOPHEN
Dosage Strength : 650MG
Approval Date : 2021-08-25
Application Number : 215486
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND IBUPRO...
Dosage Strength : 250MG;125MG
Approval Date : 2023-07-10
Application Number : 216994
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 5MG
Approval Date : 2010-06-15
Application Number : 78933
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 10MG
Approval Date : 2010-06-15
Application Number : 78933
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 5MG
Approval Date : 2010-06-15
Application Number : 78933
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 10MG
Approval Date : 2010-06-15
Application Number : 78933
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE, DELAYED REL PELLETS; ...
Proprietary Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 20MG BASE
Approval Date : 2013-12-11
Application Number : 90723
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE, DELAYED REL PELLETS; ...
Proprietary Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 30MG BASE
Approval Date : 2013-12-11
Application Number : 90723
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE, DELAYED REL PELLETS; ...
Proprietary Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 60MG BASE
Approval Date : 2013-12-11
Application Number : 90723
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE, DELAYED RELEASE; ORAL
Proprietary Name : 0
Dosage Strength : EQ 20MG BASE
Approval Date : 2023-09-29
Application Number : 217264
RX/OTC/DISCN : OTC
RLD : No
TE Code :
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