01 3DULOXETINE HYDROCHLORIDE
02 2ENTECAVIR
03 2Tofacitinib
04 5VENLAFAXINE HYDROCHLORIDE
01 12YAOPHARMA CO LTD
01 3CAPSULE, DELAYED REL PELLETS;ORAL
02 9TABLET;ORAL
01 10.5MG
02 110MG
03 11MG
04 15MG
05 1EQ 100MG BASE
06 1EQ 20MG BASE
07 1EQ 25MG BASE
08 1EQ 30MG BASE
09 1EQ 37.5MG BASE
10 1EQ 50MG BASE
11 1EQ 60MG BASE
12 1EQ 75MG BASE
01 12USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE, DELAYED REL PEL...
Brand Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2019-08-16
Application Number : 207219
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE, DELAYED REL PEL...
Brand Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 30MG BASE
Packaging :
Approval Date : 2019-08-16
Application Number : 207219
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE, DELAYED REL PEL...
Brand Name : DULOXETINE HYDROCHLORIDE
Dosage Strength : EQ 60MG BASE
Packaging :
Approval Date : 2019-08-16
Application Number : 207219
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ENTECAVIR
Dosage Strength : 0.5MG
Packaging :
Approval Date : 2019-11-04
Application Number : 212201
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ENTECAVIR
Dosage Strength : 1MG
Packaging :
Approval Date : 2019-11-04
Application Number : 212201
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : Tofacitinib
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 215552
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : Tofacitinib
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 215552
Regulatory Info :
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : VENLAFAXINE HYDROCHLORIDE
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 2015-05-28
Application Number : 202036
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : VENLAFAXINE HYDROCHLORIDE
Dosage Strength : EQ 37.5MG BASE
Packaging :
Approval Date : 2015-05-28
Application Number : 202036
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : VENLAFAXINE HYDROCHLORIDE
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 2015-05-28
Application Number : 202036
Regulatory Info : RX
Registration Country : USA
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