01 2DICHLORPHENAMIDE
02 5GLUCAGON
01 5SOLUTION;SUBCUTANEOUS
02 2TABLET;ORAL
01 20.5MG/0.1ML (0.5MG/0.1ML)
02 31MG/0.2ML (1MG/0.2ML)
03 150MG
04 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 2DISCN
02 5RX
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DARANIDE
Dosage Strength : 50MG **Federal Register ...
Approval Date : 1982-01-01
Application Number : 11366
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : KEVEYIS
Dosage Strength : 50MG
Approval Date : 2015-08-07
Application Number : 11366
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : SOLUTION; SUBCUTANEOUS
Proprietary Name : GVOKE PFS
Dosage Strength : 0.5MG/0.1ML (0.5MG/0.1ML...
Approval Date : 2019-09-10
Application Number : 212097
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; SUBCUTANEOUS
Proprietary Name : GVOKE PFS
Dosage Strength : 1MG/0.2ML (1MG/0.2ML)
Approval Date : 2019-09-10
Application Number : 212097
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; SUBCUTANEOUS
Proprietary Name : GVOKE HYPOPEN
Dosage Strength : 0.5MG/0.1ML (0.5MG/0.1ML...
Approval Date : 2019-09-10
Application Number : 212097
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; SUBCUTANEOUS
Proprietary Name : GVOKE HYPOPEN
Dosage Strength : 1MG/0.2ML (1MG/0.2ML)
Approval Date : 2019-09-10
Application Number : 212097
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; SUBCUTANEOUS
Proprietary Name : GVOKE KIT
Dosage Strength : 1MG/0.2ML (1MG/0.2ML)
Approval Date : 2021-08-20
Application Number : 212097
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
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