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01 1Aucta Pharmaceuticals

02 1Acme Lifetech

03 1Aeron Remedies

04 4Aurobindo Pharma Limited

05 2Caristar Laboratories

06 2Delius Pharmaceuticals

07 2Dycine Pharma

08 1Halewood Laboratories Pvt. Ltd

09 1Hanlim Pharmaceuticals Inc

10 3LAB.GUIDOTTI SpA

11 1Myungmoon Pharm. Co., LTD.

12 5PTC Therapeutics

13 4Sun Pharmaceutical Industries Limited

14 2Swasthya Healthcare

15 3TEOFARMA Srl

16 1Themis Medicare

17 1Tris Pharma Inc

18 1Unicor Pharmatech

19 4Upsher-Smith Laboratories

20 1Vaishali Pharma Ltd

21 1Vega Biotech Pvt. Ltd.

22 5ZRS LABS

23 1Zota Healthcare Ltd

24 4Zydus Lifesciences

25 26Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAucta is a global brand that creates better products from proven molecules.

Regulatory Info : RX

Registration Country : USA

DEFLAZACORT

Brand Name : PYQUVI

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 22.75MG/ML

Packaging :

Approval Date : 2025-06-30

Application Number : 219417

Regulatory Info : RX

Registration Country : USA

Aucta Company Banner

02

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2024-02-09

Application Number : 217123

Regulatory Info : RX

Registration Country : USA

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03

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 18MG

Packaging :

Approval Date : 2024-02-09

Application Number : 217123

Regulatory Info : RX

Registration Country : USA

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04

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 2024-02-09

Application Number : 217123

Regulatory Info : RX

Registration Country : USA

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05

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 36MG

Packaging :

Approval Date : 2024-02-09

Application Number : 217123

Regulatory Info : RX

Registration Country : USA

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06

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : EMFLAZA

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2017-02-09

Application Number : 208684

Regulatory Info : RX

Registration Country : USA

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07

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : EMFLAZA

Dosage Form : TABLET;ORAL

Dosage Strength : 18MG

Packaging :

Approval Date : 2017-02-09

Application Number : 208684

Regulatory Info : RX

Registration Country : USA

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08

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : EMFLAZA

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 2017-02-09

Application Number : 208684

Regulatory Info : RX

Registration Country : USA

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09

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : EMFLAZA

Dosage Form : TABLET;ORAL

Dosage Strength : 36MG

Packaging :

Approval Date : 2017-02-09

Application Number : 208684

Regulatory Info : RX

Registration Country : USA

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10

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : EMFLAZA

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 22.75MG/ML

Packaging :

Approval Date : 2017-02-09

Application Number : 208685

Regulatory Info : RX

Registration Country : USA

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11

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2025-03-18

Application Number : 217741

Regulatory Info : RX

Registration Country : USA

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12

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 18MG

Packaging :

Approval Date : 2025-03-18

Application Number : 217741

Regulatory Info : RX

Registration Country : USA

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13

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 2025-03-18

Application Number : 217741

Regulatory Info : RX

Registration Country : USA

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14

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 36MG

Packaging :

Approval Date : 2025-03-18

Application Number : 217741

Regulatory Info : RX

Registration Country : USA

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15

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 22.75MG/ML

Packaging :

Approval Date : 2024-04-25

Application Number : 217813

Regulatory Info : RX

Registration Country : USA

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16

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2024-11-05

Application Number : 216720

Regulatory Info : RX

Registration Country : USA

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17

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 18MG

Packaging :

Approval Date : 2024-11-05

Application Number : 216720

Regulatory Info : RX

Registration Country : USA

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18

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 2024-11-05

Application Number : 216720

Regulatory Info : RX

Registration Country : USA

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19

Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : DEFLAZACORT

Dosage Form : TABLET;ORAL

Dosage Strength : 36MG

Packaging :

Approval Date : 2024-11-05

Application Number : 216720

Regulatory Info : RX

Registration Country : USA

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Chemicals America
Not Confirmed
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Chemicals America
Not Confirmed

DEFLAZACORT

Brand Name : JAYTHARI

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2025-04-08

Application Number : 219254

Regulatory Info : RX

Registration Country : USA

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