01 2BECLOMETHASONE DIPROPIONATE; FORMOTEROL FUMARATE; GLYCOPYRROLATE
02 1BIRCH TRITERPENES
03 1CANGRELOR
04 3CLEVIDIPINE
05 5DEFERIPRONE
06 1ELAPEGADEMASE-LVLR
07 7LOMITAPIDE MESYLATE
08 10NICARDIPINE HYDROCHLORIDE
09 1OCTREOTIDE ACETATE
10 1PORACTANT ALFA
11 1TOBRAMYCIN
12 3ZILEUTON
01 2AEROSOL, METERED;INHALATION
02 1CAPSULE, DELAYED RELEASE;ORAL
03 3CAPSULE, EXTENDED RELEASE;ORAL
04 9CAPSULE;ORAL
05 3EMULSION;INTRAVENOUS
06 1GEL;TOPICAL
07 2INJECTABLE;INJECTION
08 4INJECTABLE;INTRAVENOUS
09 1POWDER;INTRAVENOUS
10 1SOLUTION;INHALATION
11 2SOLUTION;ORAL
12 1SUSPENSION;INTRATRACHEAL
13 1TABLET, EXTENDED RELEASE;ORAL
14 5TABLET;ORAL
01 10.086MG/INH;0.0049MG/INH;0.0106MG/INH
02 10.172MG/INH;0.0049MG/INH;0.0106MG/INH
03 11.6MG/ML
04 110%
05 1100MG/ML
06 1125MG/250ML (0.5MG/ML)
07 21GM
08 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 220MG/200ML (0.1MG/ML)
10 125MG/10ML (2.5MG/ML)
11 125MG/50ML (0.5MG/ML)
12 1300MG
13 1300MG/4ML
14 230MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 240MG/200ML (0.2MG/ML)
16 145MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 1500MG
18 150MG/100ML (0.5MG/ML)
19 150MG/VIAL
20 1600MG
21 1600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 280MG/ML
24 1EQ 10MG BASE
25 2EQ 20MG BASE
26 1EQ 2MG BASE
27 1EQ 30MG BASE
28 1EQ 40MG BASE
29 1EQ 5MG BASE
30 1EQ 60MG BASE
01 14DISCN
02 18RX
03 4Blank
RLD :
TE Code :
BECLOMETHASONE DIPROPIONATE; FORMOTEROL FUMARATE; GLYCOPYRROLATE
Dosage Form : AEROSOL, METERED; INHALATION
Proprietary Name : TRIMBOW
Dosage Strength : 0.086MG/INH;0.0049MG/INH...
Approval Date :
Application Number : 219622
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
BECLOMETHASONE DIPROPIONATE; FORMOTEROL FUMARATE; GLYCOPYRROLATE
Dosage Form : AEROSOL, METERED; INHALATION
Proprietary Name : TRIMBOW
Dosage Strength : 0.172MG/INH;0.0049MG/INH...
Approval Date :
Application Number : 219622
RX/OTC/DISCN :
RLD :
TE Code :
RLD : Yes
TE Code :
Dosage Form : GEL; TOPICAL
Proprietary Name : FILSUVEZ
Dosage Strength : 10%
Approval Date : 2023-12-18
Application Number : 215064
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : AP
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : KENGREAL
Dosage Strength : 50MG/VIAL
Approval Date : 2015-06-22
Application Number : 204958
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code :
Dosage Form : EMULSION; INTRAVENOUS
Proprietary Name : CLEVIPREX
Dosage Strength : 25MG/50ML (0.5MG/ML)
Approval Date : 2008-08-01
Application Number : 22156
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : EMULSION; INTRAVENOUS
Proprietary Name : CLEVIPREX
Dosage Strength : 50MG/100ML (0.5MG/ML)
Approval Date : 2008-08-01
Application Number : 22156
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : EMULSION; INTRAVENOUS
Proprietary Name : CLEVIPREX
Dosage Strength : 125MG/250ML (0.5MG/ML)
Approval Date : 2013-11-08
Application Number : 22156
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FERRIPROX
Dosage Strength : 500MG
Approval Date : 2011-10-14
Application Number : 21825
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FERRIPROX
Dosage Strength : 1GM
Approval Date : 2019-07-25
Application Number : 21825
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FERRIPROX
Dosage Strength : 1GM
Approval Date : 2020-05-19
Application Number : 212269
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
