01 1CETIRIZINE HYDROCHLORIDE
02 2GOSERELIN (GOSERELIN ACETATE)
03 2GOSERELIN ACETATE
04 2MELOXICAM
05 2ROLAPITANT HYDROCHLORIDE
06 1TELOTRISTAT ETIPRATE
07 4ZICONOTIDE ACETATE
01 1JDP
02 11TERSERA
03 2TERSERA THERAPEUTICS LLC
01 1EMULSION;INTRAVENOUS
02 2IMPLANT
03 2IMPLANT;IMPLANTATION
04 4INJECTABLE;INTRATHECAL
05 1SOLUTION;INTRAVENOUS
06 2TABLET, ORALLY DISINTEGRATING;ORAL
07 2TABLET;ORAL
01 110.8MG
02 1100MCG/1ML (100MCG/ML)
03 110MG/ML (10MG/ML)
04 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 1200MCG/2ML (100MCG/ML)
06 13.6MG
07 1500MCG/20ML (25MCG/ML)
08 1500MCG/5ML (100MCG/ML)
09 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1EQ 10.8MG BASE
11 1EQ 166.5MG BASE/92.5ML (EQ 1.8MG BASE/ML)
12 1EQ 250MG BASE
13 1EQ 3.6MG BASE
14 1EQ 90MG BASE
01 2Canada
02 12USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : QUZYTTIR
Dosage Strength : 10MG/ML (10MG/ML)
Packaging :
Approval Date : 2019-10-04
Application Number : 211415
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : IMPLANT
Brand Name : ZOLADEX
Dosage Strength : 3.6MG
Packaging : ONE DEPOT
Approval Date :
Application Number : 2049325
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : IMPLANT
Brand Name : ZOLADEX LA
Dosage Strength : 10.8MG
Packaging : ONE DEPOT
Approval Date :
Application Number : 2225905
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Dosage Form : IMPLANT;IMPLANTATION
Brand Name : ZOLADEX
Dosage Strength : EQ 3.6MG BASE
Packaging :
Approval Date : 1989-12-29
Application Number : 19726
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : IMPLANT;IMPLANTATION
Brand Name : ZOLADEX
Dosage Strength : EQ 10.8MG BASE
Packaging :
Approval Date : 1996-01-11
Application Number : 20578
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : QMIIZ ODT
Dosage Strength : 7.5MG **Federal Regist...
Packaging :
Approval Date : 2018-10-19
Application Number : 211210
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : QMIIZ ODT
Dosage Strength : 15MG **Federal Registe...
Packaging :
Approval Date : 2018-10-19
Application Number : 211210
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : VARUBI
Dosage Strength : EQ 90MG BASE
Packaging :
Approval Date : 2015-09-01
Application Number : 206500
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : EMULSION;INTRAVENOUS
Brand Name : VARUBI
Dosage Strength : EQ 166.5MG BASE/92.5ML...
Packaging :
Approval Date : 2017-10-25
Application Number : 208399
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : XERMELO
Dosage Strength : EQ 250MG BASE
Packaging :
Approval Date : 2017-02-28
Application Number : 208794
Regulatory Info : RX
Registration Country : USA
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