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01 4Athena Pharmaceutiques
02 1Allergan Aesthetics
03 8Aspen Pharmacare Holdings
04 3Strides Pharma Science
05 1ACE Pharmaceuticals BV
06 5Actavis Inc
07 8Adcock Ingram
08 1Agepha Pharma Sro
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11 5Alter Nova
12 3Alternova A / S
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14 6BRUNO FARMACEUTICI SpA
15 1BUNDY
16 1Barr Laboratories
17 1Bausch Health
18 3Bayer AG
19 4Bruno Farmaceutici S.p.A
20 1Caps Pharmaceuticals
21 3Chartwell Pharmaceuticals llc
22 1DECHRA VETERINARY PRODUCTS AS
23 1ELKINS SINN
24 2FERRANTE
25 1Farmigea
26 1Ferndale Laboratories, Inc.
27 1Forest Laboratories
28 1Fosun Pharmaceutical
29 3HALSEY
30 1HEATHER
31 1Halewood Laboratories Pvt. Ltd
32 2Hanlim Pharmaceuticals Inc
33 1Hikma Pharmaceuticals
34 2IVAX Pharmaceuticals Inc
35 1Impax Laboratories
36 1Lannett Company, Inc.
37 1MARSHALL PHARMA
38 1MIBE Arzneimittel GmbH
39 1MURO
40 2Madras Pharmaceuticals
41 1Maxheal Pharmaceuticals (India) Ltd
42 1Merck & Co
43 5Neogen N.V.
44 2Nesher Pharmaceuticals USA LLC
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46 3PHARM ASSOC
47 1PHARMOBEDIENT CNSLTG
48 1PUREPAC PHARM
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51 7Pfizer Inc
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55 2RELIANCE FORMULATION PVT. LTD
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77 1Zhejiang Xianju Pharmaceutical Co. Ltd
78 3Zim Laboratories
79 3Zota Healthcare Ltd
80 3everyLIFE Technologies
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01 10Antic-calc Tablet
02 1CREAM;TOPICAL
03 2DC Granules and Tablets
04 1EYE DROPS, SUSPENSION
05 1EYE OINTMENT
06 1Film-Coated Tablets
07 5Filmtabl
08 2Gastro Resistant Tablet
09 2Gastro-resistant tablet
10 2INJECTABLE;INJECTION
11 1Insert the pill
12 2OIN
13 1OINTMENT;OPHTHALMIC
14 2Oro-Dispersible Tablet
15 1POWDER FOR SOLUTION FOR INJECTION
16 2Powder For Solution
17 1Prednisolone 10Mg 20 Joined' Oral Use
18 1Prednisolone 2,5Mg 20 Joined' Oral Use
19 1Prednisolone 20Mg 20 Joined' Oral Use
20 1Prednisolone 5Mg 20 Joined' Oral Use
21 2SUP
22 1SUSPENSION
23 4SYR
24 2SYRUP
25 14SYRUP;ORAL
26 2Soluble Tablet
27 1Solution
28 1Solution For Intra-Articular And Intramuscular Administration
29 1Syrup
30 3TAB
31 17TABLET
32 46TABLET;ORAL
33 4TABLETT
34 6Tabl
35 12Tablet
36 10tablet
37 1Øyesalve
38 7Blank
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01 56DISCN
02 19Generic
03 4Originator
04 8RX
05 87Blank
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01 1Adco Prednisolone Syrup
02 2Biodelta Cortilen
03 1CANAURAL
04 1CHLOROPTIC-P S.O.P.
05 3CORTALONE
06 1Capsoid
07 1DELTA-CORTEF
08 2Deltacortenesol
09 2Deltacortril
10 1Deltamidrina
11 1FERNISOLONE-P
12 1HYDELTRA-TBA
13 4Idelt
14 1Lenisolone
15 1METI-DERM
16 2PRD
17 1PREDIN
18 52PREDNISOLONE
19 1PREDNISOLONE TEBUTATE
20 2PRELONE
21 5Panafcortelone
22 1Pedicort
23 1Precortalon aquosum
24 2Prednesol
25 1Prednisilone 15 Strides
26 5Prednisolon
27 5Prednisolon Altar Nova
28 3Prednisolone Alternova
29 1Prednisolone MIBE
30 3Prednisolone Pfizer
31 1Prednisolone Pilum
32 1Prednisolone Sod Succinate
33 6Prednisolone Streuli
34 2Predsolone
35 1Prelone
36 2Prelone Syrup
37 1Rheosolon
38 4Rindelt
39 1SINTISONE
40 1STERANE
41 1Scheriproct
42 1Scheriproct Oinment
43 1Scheriproct Ointment
44 2Scheriproct Suppositories
45 1Scheriproct combination pack
46 3Solone
47 1Solprene
48 2Solu-Delta-Cortef
49 2Spiricort 20
50 2Spiricort 5
51 2Spiricort 50
52 2Ultracortenol
53 1VANECTYL-P
54 25Blank
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01 10Australia
02 10Canada
03 1China
04 1Egypt
05 4France
06 1Hungary
07 15India
08 10Italy
09 1Kenya
10 13Norway
11 11South Africa
12 2South Korea
13 14Sweden
14 12Switzerland
15 64USA
16 1Venezuela
17 4Blank
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Soluble Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CHLOROPTIC-P S.O.P.
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : 1%;0.5%
Packaging :
Approval Date : 1982-01-01
Application Number : 61188
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Australia
Brand Name : Panafcortelone
Dosage Form : tablet
Dosage Strength : 1 mg
Packaging : 100
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 1MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Soluble Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Oro-Dispersible Tablet
Dosage Strength : 1MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Oro-Dispersible Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : Australia
Brand Name : Predsolone
Dosage Form : tablet
Dosage Strength : 1 mg
Packaging : 100
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Panafcortelone
Dosage Form : tablet
Dosage Strength : 5 mg
Packaging : 60
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Panafcortelone
Dosage Form : tablet
Dosage Strength : 25 mg
Packaging : 30
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Panafcortelone
Dosage Form : tablet
Dosage Strength : 5 mg
Packaging : 60
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Panafcortelone
Dosage Form : tablet
Dosage Strength : 1 mg
Packaging : 100
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Predsolone
Dosage Form : tablet
Dosage Strength : 1 mg
Packaging : 100
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Lenisolone
Dosage Form : TAB
Dosage Strength : 5mg
Packaging : 1000X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Prednisilone 15 Strides
Dosage Form : SYR
Dosage Strength : 15mg/5ml
Packaging : 50X1mg/5ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : DISCN
Registration Country : USA
Brand Name : METI-DERM
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.5%
Packaging :
Approval Date : 1982-01-01
Application Number : 10209
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 15MG/5ML
Packaging :
Approval Date : 1999-05-13
Application Number : 40323
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 15MG/5ML
Packaging :
Approval Date : 2003-02-27
Application Number : 40401
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 15MG/5ML
Packaging :
Approval Date : 1999-05-28
Application Number : 40287
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDELTRA-TBA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 10562
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 15MG/5ML
Packaging :
Approval Date : 2002-04-10
Application Number : 40364
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 5MG/5ML
Packaging :
Approval Date : 2001-10-22
Application Number : 40423
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DELTA-CORTEF
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 9987
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : STERANE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 9996
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 15MG/5ML
Packaging :
Approval Date : 2003-03-05
Application Number : 40399
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 5MG/5ML
Packaging :
Approval Date : 2005-08-25
Application Number : 40570
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 15MG/5ML
Packaging :
Approval Date : 2000-01-19
Application Number : 40322
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PREDNISOLONE
Dosage Form : SYRUP;ORAL
Dosage Strength : 15MG/5ML
Packaging :
Approval Date : 1998-05-28
Application Number : 40192
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
Dosage Form : SYRUP;ORAL
Dosage Strength : 15MG/5ML
Packaging :
Approval Date : 2003-09-10
Application Number : 40313
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF