01 1AMOXICILLIN
02 7CEPHALEXIN
03 4TRAZODONE HYDROCHLORIDE
01 4CAPSULE;ORAL
02 3FOR SUSPENSION;ORAL
03 1TABLET, EXTENDED RELEASE;ORAL
04 4TABLET;ORAL
01 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 1150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 1775MG
06 1EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
07 1EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 1EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 1EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
10 1EQ 333MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 1EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 1EQ 750MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 12DISCN
RLD : Yes
TE Code :
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : MOXATAG
Dosage Strength : 775MG
Approval Date : 2008-01-23
Application Number : 50813
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : KEFLEX
Dosage Strength : EQ 250MG BASE **Federal ...
Approval Date : 1982-01-01
Application Number : 50405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : KEFLEX
Dosage Strength : EQ 500MG BASE **Federal ...
Approval Date : 1982-01-01
Application Number : 50405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : KEFLEX
Dosage Strength : EQ 333MG BASE **Federal ...
Approval Date : 2006-05-12
Application Number : 50405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : KEFLEX
Dosage Strength : EQ 750MG BASE **Federal ...
Approval Date : 2006-05-12
Application Number : 50405
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : KEFLEX
Dosage Strength : EQ 125MG BASE/5ML **Fede...
Approval Date : 1982-01-01
Application Number : 50406
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : KEFLEX
Dosage Strength : EQ 250MG BASE/5ML **Fede...
Approval Date : 1982-01-01
Application Number : 50406
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : KEFLEX
Dosage Strength : EQ 100MG BASE/ML **Feder...
Approval Date : 1982-01-01
Application Number : 50406
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DESYREL
Dosage Strength : 50MG **Federal Register ...
Approval Date : 1982-01-01
Application Number : 18207
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DESYREL
Dosage Strength : 100MG **Federal Register...
Approval Date : 1982-01-01
Application Number : 18207
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
Pragma Pharms Llc is a supplier offers 1 products (APIs, Excipients or Intermediates).
Find a price of MANUFACTURING SITE, FACILITIES, PERSONNEL, AND GENERAL OPERATING PROCEDURES IN BLOOIELD, NEW JERSEY. bulk offered by Pragma Pharms Llc
