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List of All Manufacturers & Suppliers of MolPort-002-163-732 Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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$ API Ref.Price (USD/KG) : 851Xls
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01 2Orion Corporation

02 10Strides Pharma Science

03 12care4 ApS

04 5Accord healthcare

05 2Actavis Inc

06 4AiPing Pharmaceutical Inc

07 5Amneal Pharmaceuticals

08 1Apotex Inc

09 1Auro Pharma Inc

10 5Aurobindo Pharma Limited

11 4Avet Pharmaceuticals

12 8Bristol Myers Squibb

13 5Epic Pharma. LLC.

14 3IVAX Pharmaceuticals Inc

15 3Impax Laboratories

16 10Inventia Healthcare Limited

17 1JAMP PHARMA

18 1MINT PHARMACEUTICALS INC

19 3Nesher Pharmaceuticals USA LLC

20 4Oxford Pharm

21 1PRO DOC LIMITEE

22 3Pharmascience Inc.

23 3RISING PHARMA

24 5Rubicon Research

25 1SANIS HEALTH INC

26 5Teva Pharmaceutical Industries

27 3Unichem Laboratories Limited

28 4Unichem Pharmaceuticals USA, Inc

29 11Viatris

30 3XYZ Pharma

31 5Zydus Pharmaceuticals

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01

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buspirone hydrochloride

Brand Name : Anksilon

Dosage Form : TABLET

Dosage Strength : 10 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : RX

Registration Country : USA

BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPIRONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2014-08-25

Application Number : 202330

Regulatory Info : RX

Registration Country : USA

Strides Pharma Science

03

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buspirone hydrochloride

Brand Name : Anksilon

Dosage Form : TABLET

Dosage Strength : 5 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : RX

Registration Country : USA

BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPIRONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2014-08-25

Application Number : 202330

Regulatory Info : RX

Registration Country : USA

Strides Pharma Science

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : RX

Registration Country : USA

BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPIRONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 2014-08-25

Application Number : 202330

Regulatory Info : RX

Registration Country : USA

Strides Pharma Science

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : RX

Registration Country : USA

BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPIRONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 2014-08-25

Application Number : 202330

Regulatory Info : RX

Registration Country : USA

Strides Pharma Science

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : RX

Registration Country : USA

BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPIRONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 7.5MG

Packaging :

Approval Date : 2017-02-17

Application Number : 202330

Regulatory Info : RX

Registration Country : USA

Strides Pharma Science

08

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Buspirone Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

09

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Buspirone Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 7.5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

10

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Buspirone Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 10MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

11

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Buspirone Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 15MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

12

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Buspirone Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 30MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

13

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BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPAR

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1986-09-29

Application Number : 18731

Regulatory Info : DISCN

Registration Country : USA

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14

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BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPAR

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1986-09-29

Application Number : 18731

Regulatory Info : DISCN

Registration Country : USA

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15

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BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPAR

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-04-22

Application Number : 18731

Regulatory Info : DISCN

Registration Country : USA

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16

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BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPAR

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-04-22

Application Number : 18731

Regulatory Info : DISCN

Registration Country : USA

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17

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BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPAR

Dosage Form : CAPSULE;ORAL

Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2000-12-20

Application Number : 21190

Regulatory Info : DISCN

Registration Country : USA

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18

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BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPAR

Dosage Form : CAPSULE;ORAL

Dosage Strength : 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2000-12-20

Application Number : 21190

Regulatory Info : DISCN

Registration Country : USA

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19

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BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPAR

Dosage Form : CAPSULE;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2000-12-20

Application Number : 21190

Regulatory Info : DISCN

Registration Country : USA

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BUSPIRONE HYDROCHLORIDE

Brand Name : BUSPAR

Dosage Form : CAPSULE;ORAL

Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2000-12-20

Application Number : 21190

Regulatory Info : DISCN

Registration Country : USA

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