01 1ABBVIE
02 1ALLERGAN HERBERT
03 5ASPEN GLOBAL INC
04 1ALCON PHARMS LTD
05 1ALPHARMA US PHARMS
06 4ALVOGEN
07 5AMNEAL
08 7APOTEX
09 1BAUSCH
10 3BAUSCH AND LOMB INC
11 3BIONPHARMA
12 1CHARTWELL MOLECULAR
13 1CHARTWELL RX
14 7COREPHARMA
15 1DEXCEL
16 1DR REDDYS
17 1EYEPOINT PHARMS
18 3HARROW EYE
19 10HIKMA
20 1IMPAX LABS
21 1KANCHAN HLTHCARE
22 1KEY THERAP
23 10MERCK
24 3NOVARTIS
25 6NOVITIUM PHARMA
26 1OCULAR THERAPEUTIX
27 2PADAGIS US
28 1PANGEA
29 2PHARMAFAIR
30 1PHARMOBEDIENT
31 1PHARMOBEDIENT CNSLTG
32 1PHOENIX LABS NY
33 2PRASCO
34 1PVT FORM
35 1RISING
36 1ROXANE
37 4SANDOZ
38 1SENTISS
39 4SOLVAY
40 1SUN PHARM
41 8SUN PHARM INDUSTRIES
42 2UPSHER SMITH
43 1UPSHER SMITH LABS
44 8WATSON LABS
45 1WATSON LABS TEVA
46 1WHITEWORTH TOWN PLSN
47 7ZYDUS LIFESCIENCES
01 2AEROSOL;TOPICAL
02 1CONCENTRATE;ORAL
03 7ELIXIR;ORAL
04 1GEL;TOPICAL
05 1IMPLANT;INTRAVITREAL
06 3INJECTABLE;INJECTION
07 1INSERT;OPHTHALMIC
08 6OINTMENT;OPHTHALMIC
09 1SOLUTION;ORAL
10 13SUSPENSION/DROPS;OPHTHALMIC
11 6SUSPENSION/DROPS;OTIC
12 1SUSPENSION;INTRAOCULAR
13 88TABLET;ORAL
01 57DISCN
02 73RX
03 1Blank
01 1AEROSEB-DEX
02 1CIPRODEX
03 5CIPROFLOXACIN AND DEXAMETHASONE
04 1DECADERM
05 7DECADRON
06 1DECADRON-LA
07 1DECASPRAY
08 2DEXACIDIN
09 80DEXAMETHASONE
10 2DEXAMETHASONE ACETATE
11 1DEXAMETHASONE INTENSOL
12 3DEXASPORIN
13 1DEXONE 0.5
14 1DEXONE 0.75
15 1DEXONE 1.5
16 1DEXONE 4
17 1DEXTENZA
18 1DEXYCU KIT
19 1HEMADY
20 5HEXADROL
21 1MAXIDEX
22 3MAXITROL
23 3NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE
24 1OZURDEX
25 2TOBRADEX
26 1TOBRADEX ST
27 3TOBRAMYCIN AND DEXAMETHASONE
01 101No
02 29Yes
03 1Blank
RLD : Yes
TE Code :
Brand Name : OZURDEX
Dosage Form : IMPLANT;INTRAVITREAL
Dosage Strength : 0.7MG
Approval Date : 2009-06-17
Application Number : 22315
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : AEROSEB-DEX
Dosage Form : AEROSOL;TOPICAL
Dosage Strength : 0.01% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 83296
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HEXADROL
Dosage Form : ELIXIR;ORAL
Dosage Strength : 0.5MG/5ML
Approval Date : 1982-01-01
Application Number : 12674
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HEXADROL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.5MG
Approval Date : 1982-01-01
Application Number : 12675
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HEXADROL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.75MG
Approval Date : 1982-01-01
Application Number : 12675
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HEXADROL
Dosage Form : TABLET;ORAL
Dosage Strength : 1.5MG
Approval Date : 1982-01-01
Application Number : 12675
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : HEXADROL
Dosage Form : TABLET;ORAL
Dosage Strength : 4MG
Approval Date : 1982-01-01
Application Number : 12675
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : DECADRON
Dosage Form : TABLET;ORAL
Dosage Strength : 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 11664
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DECADRON
Dosage Form : TABLET;ORAL
Dosage Strength : 0.75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 11664
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DECADRON
Dosage Form : TABLET;ORAL
Dosage Strength : 1.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 11664
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
