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01 7Aspen Pharmacare Holdings

02 1Mission | CDMO

03 1Actavis Inc

04 3Advanz Pharma

05 2Alcon Inc

06 2Amneal Pharmaceuticals

07 8Bausch & Lomb Incorporated

08 1Bayer AG

09 1CONCORDIA PHARMS INC

10 1Chartwell Pharmaceuticals llc

11 1ENDO OPERATIONS

12 4Edenbridge Pharmaceuticals

13 3Epic Pharma. LLC.

14 1Genus Lifesciences

15 1Hikma Pharmaceuticals

16 3Merck & Co

17 1Mercury Laboratories

18 2Nesher Pharmaceuticals USA LLC

19 3Novartis Pharmaceuticals Corporation

20 5PHARM ASSOC

21 1PHARMOBEDIENT

22 1PHARMOBEDIENT CNSLTG

23 3Pharmascience Inc.

24 3Rising Pharmaceuticals Inc

25 4SOLA BARNES HIND

26 1Seton Pharmaceuticals

27 1Vintage Pharmaceuticals-Charlotte

28 1WE PHARMS

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PharmaCompass

01

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BioAsia
Not Confirmed

prednisolone sodium phosphate

Brand Name : Redipred

Dosage Form : oral

Dosage Strength : 5 mg/mL

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Aspen API Comapny Banner

02

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BioAsia
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.

Regulatory Info : RX

Registration Country : USA

PREDNISOLONE SODIUM PHOSPHATE

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

Mission Pharmacal

03

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BioAsia
Not Confirmed

prednisolone sodium phosphate

Brand Name : PredMix

Dosage Form : oral

Dosage Strength : 5 mg/mL

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Aspen API Comapny Banner

04

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BioAsia
Not Confirmed

prednisolone sodium phosphate

Brand Name : Predsol

Dosage Form :

Dosage Strength : 20 mg/100 mL

Packaging : 7

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Aspen API Comapny Banner

05

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BioAsia
Not Confirmed

prednisolone sodium phosphate

Brand Name : Predsol

Dosage Form :

Dosage Strength : 5 mg

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Aspen API Comapny Banner

06

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BioAsia
Not Confirmed

prednisolone sodium phosphate

Brand Name : Redipred

Dosage Form : oral

Dosage Strength : 5 mg/mL

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Aspen API Comapny Banner

07

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BioAsia
Not Confirmed

prednisolone sodium phosphate

Brand Name : PredMix

Dosage Form : oral

Dosage Strength : 5 mg/mL

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

Aspen API Comapny Banner

08

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BioAsia
Not Confirmed

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

Aspen API Comapny Banner

09

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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10

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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11

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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12

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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13

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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14

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

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

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15

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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16

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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17

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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18

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

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

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19

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

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

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20

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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21

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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22

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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23

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

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

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24

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

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

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25

PHARM ASSOC

U.S.A
BioAsia
Not Confirmed
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PHARM ASSOC

U.S.A
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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26

PHARM ASSOC

U.S.A
BioAsia
Not Confirmed
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PHARM ASSOC

U.S.A
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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27

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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28

PHARMOBEDIENT CNSLTG

Country
BioAsia
Not Confirmed
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PHARMOBEDIENT CNSLTG

Country
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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29

WE PHARMS

Country
BioAsia
Not Confirmed
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WE PHARMS

Country
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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30

PHARMOBEDIENT

Country
BioAsia
Not Confirmed
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PHARMOBEDIENT

Country
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BioAsia
Not Confirmed

PREDNISOLONE SODIUM PHOSPHATE

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

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