01 1BENZYL ALCOHOL
02 1CEFIDEROCOL SULFATE TOSYLATE
03 2DORIPENEM
04 1SULFAMETHOXAZOLE
05 2SULFAMETHOXAZOLE; TRIMETHOPRIM
06 4TACRINE HYDROCHLORIDE
07 1TRAMADOL HYDROCHLORIDE
01 4CAPSULE;ORAL
02 2INJECTABLE;INTRAVENOUS
03 1LOTION;TOPICAL
04 1POWDER;INTRAVENOUS
05 1TABLET, ORALLY DISINTEGRATING;ORAL
06 3TABLET;ORAL
01 1250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 1400MG;80MG
03 15% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 1500MG
05 1500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 150MG
07 1800MG;160MG
08 1EQ 10MG BASE
09 1EQ 1GM BASE/VIAL
10 1EQ 20MG BASE
11 1EQ 30MG BASE
12 1EQ 40MG BASE
01 11DISCN
02 1RX
RLD : Yes
TE Code :
Dosage Form : LOTION; TOPICAL
Proprietary Name : ULESFIA
Dosage Strength : 5% **Federal Register de...
Approval Date : 2009-04-09
Application Number : 22129
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : FETROJA
Dosage Strength : EQ 1GM BASE/VIAL
Approval Date : 2019-11-14
Application Number : 209445
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INTRAVENOUS
Proprietary Name : DORIBAX
Dosage Strength : 500MG/VIAL **Federal Reg...
Approval Date : 2007-10-12
Application Number : 22106
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INTRAVENOUS
Proprietary Name : DORIBAX
Dosage Strength : 250MG/VIAL **Federal Reg...
Approval Date : 2010-10-05
Application Number : 22106
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : UROBAK
Dosage Strength : 500MG
Approval Date : 1982-01-01
Application Number : 87307
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
SULFAMETHOXAZOLE; TRIMETHOPRIM
Dosage Form : TABLET; ORAL
Proprietary Name : UROPLUS SS
Dosage Strength : 400MG;80MG
Approval Date : 1987-09-28
Application Number : 71815
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
SULFAMETHOXAZOLE; TRIMETHOPRIM
Dosage Form : TABLET; ORAL
Proprietary Name : UROPLUS DS
Dosage Strength : 800MG;160MG
Approval Date : 1987-09-28
Application Number : 71816
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : COGNEX
Dosage Strength : EQ 10MG BASE
Approval Date : 1993-09-09
Application Number : 20070
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : COGNEX
Dosage Strength : EQ 20MG BASE
Approval Date : 1993-09-09
Application Number : 20070
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : COGNEX
Dosage Strength : EQ 30MG BASE
Approval Date : 1993-09-09
Application Number : 20070
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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