01 2Orion Corporation
02 10Strides Pharma Science
03 12care4 ApS
04 1AMBICARE PHARMACEUTICALS INC.
05 5Accord healthcare
06 2Actavis Inc
07 4AiPing Pharmaceutical Inc
08 5Amneal Pharmaceuticals
09 1Apotex Inc
10 1Auro Pharma Inc
11 5Aurobindo Pharma Limited
12 4Avet Pharmaceuticals
13 8Bristol Myers Squibb
14 5Epic Pharma. LLC.
15 3IVAX Pharmaceuticals Inc
16 3Impax Laboratories
17 10Inventia Healthcare Limited
18 1JAMP PHARMA
19 1MINT PHARMACEUTICALS INC
20 3Nesher Pharmaceuticals USA LLC
21 4Oxford Pharm
22 1PRO DOC LIMITEE
23 3Pharmascience Inc.
24 3Rising Pharmaceuticals Inc
25 5Rubicon Research
26 1SANIS HEALTH INC
27 5Teva Pharmaceutical Industries
28 3Unichem Laboratories Limited
29 4Unichem Pharmaceuticals USA, Inc
30 11Viatris
31 3XYZ Pharma
32 5Zydus Pharmaceuticals
01 4CAPSULE;ORAL
02 18TABLET
03 88TABLET;ORAL
04 13Tablet
01 5Countries Registered In: Ready formulation as per US RLD
02 29DISCN
03 3Generic
04 2Prescription
05 63RX
06 21Blank
01 1AMB-BUSPIRONE
02 1APO-BUSPIRONE
03 1AURO-BUSPIRONE
04 2Anksilon
05 8BUSPAR
06 1BUSPIRONE
07 84BUSPIRONE HYDROCHLORIDE
08 1Buspirone 2care4
09 2Buspirone Actavis
10 2Buspirone Mylan
11 1JAMP BUSPIRONE
12 1MINT-BUSPIRONE
13 3PMS-BUSPIRONE
14 1PRO-BUSPIRONE
15 1TEVA-BUSPIRONE
16 13Blank
01 11Canada
02 13India
03 7Sweden
04 92USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Anksilon
Dosage Form : TABLET
Dosage Strength : 10 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info :
Registration Country : Sweden
Brand Name : Anksilon
Dosage Form : TABLET
Dosage Strength : 5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
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 :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 7.5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 15MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 30MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2001-03-28
Application Number : 74253
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2001-03-28
Application Number : 74253
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG
Packaging :
Approval Date : 2002-03-13
Application Number : 74253
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2002-02-28
Application Number : 75022
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2002-02-28
Application Number : 75022
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG
Packaging :
Approval Date : 2002-02-28
Application Number : 75022
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 2004-03-25
Application Number : 75022
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2002-03-14
Application Number : 75119
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2002-03-14
Application Number : 75119
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BUSPIRONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG
Packaging :
Approval Date : 2003-01-23
Application Number : 75119
Regulatory Info : DISCN
Registration Country : USA
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