pred forte | All | Licensing, EU CTD Dossiers, Formulation Suppliers

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U.S.A

Regulatory Info : RX

Registration Country : USA

PREDNISOLONE ACETATE

Brand Name : PRED FORTE

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : 1%

Packaging :

Approval Date : 1982-01-01

Application Number : 17011

Regulatory Info : RX

Registration Country : USA

Portfolio PDF

Product Web Link

Corporate PDF

02

Allergan Aesthetics

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U.S.A

Regulatory Info : DISCN

Registration Country : USA

PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

Brand Name : BLEPHAMIDE

Dosage Form : SUSPENSION;OPHTHALMIC

Dosage Strength : 0.2%;10%

Packaging :

Approval Date : 1982-01-01

Application Number : 12813

Regulatory Info : DISCN

Registration Country : USA

Portfolio PDF

Product Web Link

Corporate PDF

03

AbbVie Inc

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U.S.A

Regulatory Info : RX

Registration Country : USA

PREDNISOLONE ACETATE

Brand Name : PRED MILD

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : 0.12%

Packaging :

Approval Date : 1982-01-01

Application Number : 17100

Regulatory Info : RX

Registration Country : USA

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Product Web Link

Corporate PDF

04

AbbVie Inc

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U.S.A

Regulatory Info :

Registration Country : Switzerland

Prednisone acetates

Brand Name : Pred Forte

Dosage Form : Gtt Opht

Dosage Strength : 1%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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Product Web Link

Corporate PDF

05

AbbVie Inc

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U.S.A

Regulatory Info : Originator

Registration Country : South Africa

Prednisolone acetate

Brand Name : Pred Forte Sterile Eye Suspension

Dosage Form : OPD

Dosage Strength : 10mg/ml

Packaging : 5X1mg/ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Portfolio PDF

Product Web Link

Corporate PDF

06

AbbVie Inc

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U.S.A

Regulatory Info : Originator

Registration Country : South Africa

Prednisolone acetate

Brand Name : Pred Mild Sterile Eye Suspension

Dosage Form : OPD

Dosage Strength : 5mg/ml

Packaging : 5X1mg/ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Portfolio PDF

Product Web Link

Corporate PDF

07

AbbVie Inc

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U.S.A

Regulatory Info :

Registration Country : Canada

PREDNISOLONE ACETATE

Brand Name : PRED FORTE

Dosage Form : SUSPENSION

Dosage Strength : 1%/W/V

Packaging : 1ML/5ML/10ML

Approval Date :

Application Number : 301175

Regulatory Info :

Registration Country : Canada

Portfolio PDF

Product Web Link

Corporate PDF

08

Allergan Aesthetics

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U.S.A

Regulatory Info : DISCN

Registration Country : USA

NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PREDNISOLONE ACETATE

Brand Name : POLY-PRED

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.35% BASE;10,000 UNITS/ML;0.5%

Packaging :

Approval Date : 1982-01-01

Application Number : 50081

Regulatory Info : DISCN

Registration Country : USA

Portfolio PDF

Product Web Link

Corporate PDF

09

Allergan Aesthetics

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U.S.A

Regulatory Info : DISCN

Registration Country : USA

GENTAMICIN SULFATE; PREDNISOLONE ACETATE

Brand Name : PRED-G

Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

Dosage Strength : EQ 0.3% BASE;1%

Packaging :

Approval Date : 1988-06-10

Application Number : 50586

Regulatory Info : DISCN

Registration Country : USA

Portfolio PDF

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Corporate PDF

10

Allergan Aesthetics

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U.S.A

Regulatory Info : DISCN

Registration Country : USA

GENTAMICIN SULFATE; PREDNISOLONE ACETATE

Brand Name : PRED-G

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : EQ 0.3% BASE;0.6%

Packaging :

Approval Date : 1989-12-01

Application Number : 50612

Regulatory Info : DISCN

Registration Country : USA

Portfolio PDF

Product Web Link

Corporate PDF

11

Allergan Aesthetics

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

U.S.A

Regulatory Info : DISCN

Registration Country : USA

PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

Brand Name : BLEPHAMIDE S.O.P.

Dosage Form : OINTMENT;OPHTHALMIC

Dosage Strength : 0.2%;10%

Packaging :

Approval Date : 1986-12-03

Application Number : 87748

Regulatory Info : DISCN

Registration Country : USA

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12

Bayer AG

Germany

The Aesthetic Show

Not Confirmed

13

Bayer AG

Germany

The Aesthetic Show

Not Confirmed

14

Bayer AG

Germany

The Aesthetic Show

Not Confirmed

15

Harrow

The Aesthetic Show

Not Confirmed

16

Pfizer Inc

The Aesthetic Show

Not Confirmed

17

Pfizer Inc

The Aesthetic Show

Not Confirmed

18

Sandoz B2B

Switzerland

The Aesthetic Show

Not Confirmed

19

Taro Pharmaceutical Industries

The Aesthetic Show

Not Confirmed

20

Taro Pharmaceutical Industries