01 1BIRCH TRITERPENES
02 1CANGRELOR
03 3CLEVIDIPINE
04 5DEFERIPRONE
05 1ELAPEGADEMASE-LVLR
06 6LOMITAPIDE MESYLATE
07 10NICARDIPINE HYDROCHLORIDE
08 1OCTREOTIDE ACETATE
09 1PORACTANT ALFA
10 1TOBRAMYCIN
11 3ZILEUTON
01 1CAPSULE, DELAYED RELEASE;ORAL
02 3CAPSULE, EXTENDED RELEASE;ORAL
03 8CAPSULE;ORAL
04 3EMULSION;INTRAVENOUS
05 1GEL;TOPICAL
06 2INJECTABLE;INJECTION
07 4INJECTABLE;INTRAVENOUS
08 1POWDER;INTRAVENOUS
09 1SOLUTION;INHALATION
10 2SOLUTION;ORAL
11 1SUSPENSION;INTRATRACHEAL
12 1TABLET, EXTENDED RELEASE;ORAL
13 5TABLET;ORAL
01 11.6MG/ML
02 110%
03 1100MG/ML
04 1125MG/250ML (0.5MG/ML)
05 21GM
06 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 220MG/200ML (0.1MG/ML)
08 125MG/10ML (2.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
09 125MG/50ML (0.5MG/ML)
10 1300MG
11 1300MG/4ML
12 230MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
13 240MG/200ML (0.2MG/ML)
14 145MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 1500MG
16 150MG/100ML (0.5MG/ML)
17 150MG/VIAL
18 1600MG
19 1600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 280MG/ML
22 1EQ 10MG BASE
23 2EQ 20MG BASE
24 1EQ 30MG BASE
25 1EQ 40MG BASE
26 1EQ 5MG BASE
27 1EQ 60MG BASE
01 13DISCN
02 18RX
03 2Blank
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 :
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 :
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 : AB
Dosage Form : TABLET; ORAL
Proprietary Name : FERRIPROX
Dosage Strength : 500MG
Approval Date : 2011-10-14
Application Number : 21825
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
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 : SOLUTION; ORAL
Proprietary Name : FERRIPROX
Dosage Strength : 100MG/ML
Approval Date : 2015-09-09
Application Number : 208030
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; ORAL
Proprietary Name : FERRIPROX
Dosage Strength : 80MG/ML
Approval Date : 2018-04-20
Application Number : 208030
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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 :
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