01 7Aspen Pharmacare Holdings
02 1Mission | CDMO
03 1Actavis Inc
04 3Advanz Pharma
05 2Alcon Inc
06 2Amneal Pharmaceuticals
07 1Ananta Medicare
08 8Bausch & Lomb Incorporated
09 1Bayer AG
10 1Chartwell Pharmaceuticals llc
11 1Concordia Labs Inc
12 4Edenbridge Pharmaceuticals
13 1Endo International
14 3Epic Pharma. LLC.
15 1Genus Lifesciences
16 1Hikma Pharmaceuticals
17 3Merck & Co
18 1Mercury Laboratories
19 2Nesher Pharmaceuticals USA LLC
20 3Novartis Pharmaceuticals Corporation
21 5PHARM ASSOC
22 1PHARMOBEDIENT
23 1PHARMOBEDIENT CNSLTG
24 3Pharmascience Inc.
25 3Rising Pharmaceuticals Inc
26 4SOLA BARNES HIND
27 1Seton Pharmaceuticals
28 1Vintage Pharmaceuticals-Charlotte
29 1WE PHARMS
01 2DROPS
02 1Drops
03 2INJECTABLE;INJECTION
04 1OINTMENT;OPHTHALMIC
05 1OINTMENT;OPHTHALMIC, OTIC
06 1OPD
07 2SOLUTION
08 19SOLUTION/DROPS;OPHTHALMIC
09 24SOLUTION;ORAL
10 1SYR
11 1Soluble Tablet
12 6TABLET, ORALLY DISINTEGRATING;ORAL
13 4oral
14 2Blank
01 37DISCN
02 1Generic
03 1Originator
04 4Prescription
05 16RX
06 8Blank
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 1Prednisolone Phosphate
19 2Predsol
20 2Redipred
21 2SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
22 1SULSTER
23 1VASOCIDIN
24 1Blank
01 6Australia
02 4Canada
03 2India
04 2South Africa
05 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 : 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 : 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
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 : 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 : 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
