01 7Aspen Pharmacare Holdings
02 1Mission | CDMO
03 1Actavis Inc
04 2Alcon Inc
05 2Amneal Pharmaceuticals
06 8Bausch & Lomb Incorporated
07 1Bayer AG
08 4CONCORDIA PHARMS INC
09 1Chartwell Pharmaceuticals llc
10 1ENDO OPERATIONS
11 4Edenbridge Pharmaceuticals
12 3Epic Pharma. LLC.
13 1Genus Lifesciences
14 1Hikma Pharmaceuticals
15 3Merck & Co
16 2Nesher Pharmaceuticals USA LLC
17 3Novartis Pharmaceuticals Corporation
18 5PHARM ASSOC
19 1PHARMOBEDIENT
20 1PHARMOBEDIENT CNSLTG
21 3Pharmascience Inc.
22 3Rising Pharmaceuticals Inc
23 4SOLA BARNES HIND
24 1Seton Pharmaceuticals
25 1Vintage Pharmaceuticals-Charlotte
26 1WE PHARMS
01 2DROPS
02 2INJECTABLE;INJECTION
03 1OINTMENT;OPHTHALMIC
04 1OINTMENT;OPHTHALMIC, OTIC
05 1OPD
06 2SOLUTION
07 19SOLUTION/DROPS;OPHTHALMIC
08 24SOLUTION;ORAL
09 1SYR
10 6TABLET, ORALLY DISINTEGRATING;ORAL
11 4oral
12 2Blank
01 37DISCN
02 1Generic
03 1Originator
04 4Prescription
05 16RX
06 6Blank
01 1Aspelone
02 2HYDELTRASOL
03 1INFLAMASE FORTE
04 1INFLAMASE MILD
05 1METRETON
06 1MINIMS PREDNISOLONE SODIUM PHOSPHATE
07 1MINIMS PREDNISOLONE SODIUM PHOSPHATE 0,5 %
08 1NEO-HYDELTRASOL
09 1ORAPRED
10 3ORAPRED ODT
11 1PEDIAPRED
12 2PMS-PREDNISOLONE
13 1PMS-PREDNISOLONE SOD PHOS OPH SOL FORTE 1%
14 1PREDAIR
15 1PREDAIR FORTE
16 36PREDNISOLONE SODIUM PHOSPHATE
17 2PredMix
18 2Predsol
19 2Redipred
20 2SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
21 1SULSTER
22 1VASOCIDIN
01 6Australia
02 4Canada
03 2South Africa
04 53USA
Regulatory Info : Generic
Registration Country : South Africa
Prednisolone Sodium Phosphate Which Is Equivalent To 15 Mg Prednisolone Base
Brand Name : Aspelone
Dosage Form : SYR
Dosage Strength : 15mg/ 5ml
Packaging : 50X1mg/ 5ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.
Regulatory Info : RX
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 25MG BASE/5ML
Packaging :
Approval Date : 2010-09-13
Application Number : 91396
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Australia
Brand Name : Redipred
Dosage Form : oral
Dosage Strength : 5 mg/mL
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : PredMix
Dosage Form : oral
Dosage Strength : 5 mg/mL
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Predsol
Dosage Form :
Dosage Strength : 20 mg/100 mL
Packaging : 7
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Predsol
Dosage Form :
Dosage Strength : 5 mg
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Redipred
Dosage Form : oral
Dosage Strength : 5 mg/mL
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : PredMix
Dosage Form : oral
Dosage Strength : 5 mg/mL
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.11% PHOSPHATE
Packaging :
Approval Date : 1994-07-29
Application Number : 40065
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.9% PHOSPHATE
Packaging :
Approval Date : 1994-07-29
Application Number : 40070
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Brand Name : SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.23% PHOSPHATE;10%
Packaging :
Approval Date : 1995-12-29
Application Number : 74449
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 15MG BASE/5ML
Packaging :
Approval Date : 2002-07-12
Application Number : 75250
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 5MG BASE/5ML
Packaging :
Approval Date : 2004-05-25
Application Number : 75988
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ORAPRED ODT
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2006-06-01
Application Number : 21959
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ORAPRED ODT
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : EQ 15MG BASE
Packaging :
Approval Date : 2006-06-01
Application Number : 21959
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ORAPRED ODT
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : EQ 30MG BASE
Packaging :
Approval Date : 2006-06-01
Application Number : 21959
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ORAPRED
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 15MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2000-12-14
Application Number : 75117
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Brand Name : SULSTER
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.23% PHOSPHATE;10%
Packaging :
Approval Date : 1996-07-30
Application Number : 74511
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Brand Name : SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.23% PHOSPHATE;10%
Packaging :
Approval Date : 1993-05-27
Application Number : 73630
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 5MG BASE/5ML
Packaging :
Approval Date : 2003-03-26
Application Number : 75183
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDELTRASOL
Dosage Form : OINTMENT;OPHTHALMIC, OTIC
Dosage Strength : EQ 0.25% PHOSPHATE
Packaging :
Approval Date : 1982-01-01
Application Number : 11028
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDELTRASOL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG PHOSPHATE/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 11583
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NEOMYCIN SULFATE; PREDNISOLONE SODIUM PHOSPHATE
Brand Name : NEO-HYDELTRASOL
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 3.5MG BASE/GM;EQ 0.25% PHOSPHATE
Packaging :
Approval Date : 1982-01-01
Application Number : 50378
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Brand Name : VASOCIDIN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.23% PHOSPHATE;10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1988-08-26
Application Number : 18988
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 5MG BASE/5ML
Packaging :
Approval Date : 2002-12-23
Application Number : 76123
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 15MG BASE/5ML
Packaging :
Approval Date : 2005-04-25
Application Number : 76913
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PEDIAPRED
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 5MG BASE/5ML
Packaging :
Approval Date : 1986-05-28
Application Number : 19157
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 5MG BASE/5ML
Packaging :
Approval Date : 2002-06-28
Application Number : 75099
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 5MG BASE/5ML
Packaging :
Approval Date : 2002-12-23
Application Number : 75181
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE SODIUM PHOSPHATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 15MG BASE/5ML
Packaging :
Approval Date : 2004-10-04
Application Number : 76895
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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