30 Jun 2025
// FDA
03 Feb 2025
// FDA
11 Mar 2024
// DRUG STORE NEWS
Latest Content by PharmaCompass
Reset all filters
01 1ARFORMOTEROL TARTRATE
02 1DEFLAZACORT
03 3LACOSAMIDE
04 1OXCARBAZEPINE
05 2SAPROPTERIN DIHYDROCHLORIDE
06 1VIGABATRIN
Reset all filters
01 3CAPSULE, EXTENDED RELEASE;ORAL
02 1FOR SOLUTION;ORAL
03 2POWDER;ORAL
04 1SOLUTION;INHALATION
05 2SUSPENSION;ORAL
Reset all filters
01 1100MG
02 1100MG/PACKET
03 1150MG
04 1200MG
05 122.75MG/ML
06 1300MG/5ML
07 2500MG/PACKET
08 1EQ 0.015MG BASE/2ML
Reset all filters
01 9RX
RLD : No
TE Code : AN
Dosage Form : SOLUTION; INHALATION
Proprietary Name : ARFORMOTEROL TARTRATE
Dosage Strength : EQ 0.015MG BASE/2ML
Approval Date : 2025-02-03
Application Number : 218380
RX/OTC/DISCN : RX
RLD : No
TE Code : AN
RLD : No
TE Code : AB
Dosage Form : SUSPENSION; ORAL
Proprietary Name : PYQUVI
Dosage Strength : 22.75MG/ML
Approval Date : 2025-06-30
Application Number : 219417
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...
Proprietary Name : MOTPOLY XR
Dosage Strength : 100MG
Approval Date : 2023-05-04
Application Number : 216185
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...
Proprietary Name : MOTPOLY XR
Dosage Strength : 150MG
Approval Date : 2023-05-04
Application Number : 216185
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...
Proprietary Name : MOTPOLY XR
Dosage Strength : 200MG
Approval Date : 2023-05-04
Application Number : 216185
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code : AB
Dosage Form : SUSPENSION; ORAL
Proprietary Name : OXCARBAZEPINE
Dosage Strength : 300MG/5ML
Approval Date : 2022-11-30
Application Number : 215332
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : POWDER; ORAL
Proprietary Name : ZELVYSIA
Dosage Strength : 100MG/PACKET
Approval Date : 2025-04-29
Application Number : 218645
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : POWDER; ORAL
Proprietary Name : ZELVYSIA
Dosage Strength : 500MG/PACKET
Approval Date : 2025-04-29
Application Number : 218645
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AA
Dosage Form : FOR SOLUTION; ORAL
Proprietary Name : VIGADRONE
Dosage Strength : 500MG/PACKET
Approval Date : 2018-06-21
Application Number : 210196
RX/OTC/DISCN : RX
RLD : No
TE Code : AA