01 2Ajanta Pharma Limited
02 3Almirall
03 2Johnson & Johnson Innovative Medicine
04 3ORIFARM GROUP AS
05 1PRO DOC LIMITEE
06 2Paranova Group AS
07 3Pharmachim AB
08 1SANIS HEALTH INC
09 1Sandoz B2B
10 3Teva Pharmaceutical Industries
11 4Viatris
01 9FILM COATED PILL
02 2Filmtabl
03 6TABLET
04 8TABLET;ORAL
01 2DISCN
02 6Prescription
03 6RX
04 11Blank
01 2ALMOTRIPTAN
02 6ALMOTRIPTAN MALATE
03 2AXERT
04 11Almogran
05 2MYLAN-ALMOTRIPTAN
06 1SANDOZ ALMOTRIPTAN
07 1TEVA-ALMOTRIPTAN
01 6Canada
02 9Sweden
03 2Switzerland
04 8USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ALMOTRIPTAN MALATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 6.25MG BASE
Packaging :
Approval Date : 2016-03-03
Application Number : 205523
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ALMOTRIPTAN MALATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 12.5MG BASE
Packaging :
Approval Date : 2016-03-03
Application Number : 205523
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Switzerland
Brand Name : Almogran
Dosage Form : Filmtabl
Dosage Strength : 12.5mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Almogran
Dosage Form : Filmtabl
Dosage Strength : 12.5mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AXERT
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 6.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2001-05-07
Application Number : 21001
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AXERT
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2001-05-07
Application Number : 21001
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info : Prescription
Registration Country : Canada
ALMOTRIPTAN (ALMOTRIPTAN MALATE)
Brand Name : ALMOTRIPTAN
Dosage Form : TABLET
Dosage Strength : 12.5MG
Packaging : 6
Approval Date :
Application Number : 2424029
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
ALMOTRIPTAN (ALMOTRIPTAN MALATE)
Brand Name : SANDOZ ALMOTRIPTAN
Dosage Form : TABLET
Dosage Strength : 12.5MG
Packaging : 06-Oct
Approval Date :
Application Number : 2405334
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
ALMOTRIPTAN (ALMOTRIPTAN MALATE)
Brand Name : ALMOTRIPTAN
Dosage Form : TABLET
Dosage Strength : 12.5MG
Packaging : 6
Approval Date :
Application Number : 2466821
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Brand Name : ALMOTRIPTAN MALATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 6.25MG BASE
Packaging :
Approval Date : 2015-07-07
Application Number : 78027
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ALMOTRIPTAN MALATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 12.5MG BASE
Packaging :
Approval Date : 2015-07-07
Application Number : 78027
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
ALMOTRIPTAN (ALMOTRIPTAN MALATE)
Brand Name : TEVA-ALMOTRIPTAN
Dosage Form : TABLET
Dosage Strength : 12.5MG
Packaging : 6
Approval Date :
Application Number : 2434849
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Brand Name : ALMOTRIPTAN MALATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 6.25MG BASE
Packaging :
Approval Date : 2015-11-09
Application Number : 205171
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ALMOTRIPTAN MALATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 12.5MG BASE
Packaging :
Approval Date : 2015-11-09
Application Number : 205171
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
ALMOTRIPTAN (ALMOTRIPTAN MALATE)
Brand Name : MYLAN-ALMOTRIPTAN
Dosage Form : TABLET
Dosage Strength : 12.5MG
Packaging :
Approval Date :
Application Number : 2398443
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
ALMOTRIPTAN (ALMOTRIPTAN MALATE)
Brand Name : MYLAN-ALMOTRIPTAN
Dosage Form : TABLET
Dosage Strength : 6.25MG
Packaging : 6
Approval Date :
Application Number : 2398435
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Sweden
Brand Name : Almogran
Dosage Form : FILM COATED PILL
Dosage Strength : 12.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
