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01 1BUPROPION HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE
02 1MELOXICAM; RIZATRIPTAN BENZOATE
03 2SOLRIAMFETOL (SOLRIAMFETOL HYDROCHLORIDE)
04 2SOLRIAMFETOL HYDROCHLORIDE
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01 2AXSOME
02 2AXSOME MALTA
03 2AXSOME MALTA LTD.
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01 2TABLET
02 1TABLET, EXTENDED RELEASE;ORAL
03 3TABLET;ORAL
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01 1105MG;45MG
02 1150MG
03 120MG;EQ 10MG BASE
04 175MG
05 1EQ 150MG BASE
06 1EQ 75MG BASE
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01 2Canada
02 4USA
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Regulatory Info : RX
Registration Country : USA
Bupropion Hydrochloride; Dextromethorphan Hydrobromide
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : AUVELITY
Dosage Strength : 105MG;45MG
Packaging :
Approval Date : 2022-08-18
Application Number : 215430
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Meloxicam; Rizatriptan Benzoate
Dosage Form : TABLET;ORAL
Brand Name : SYMBRAVO
Dosage Strength : 20MG;EQ 10MG BASE
Packaging :
Approval Date : 2025-01-30
Application Number : 215431
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Prescription
Registration Country : Canada
SOLRIAMFETOL (SOLRIAMFETOL HYDROCHLORIDE)
Dosage Form : TABLET
Brand Name : SUNOSI
Dosage Strength : 75MG
Packaging :
Approval Date :
Application Number : 2515814
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
SOLRIAMFETOL (SOLRIAMFETOL HYDROCHLORIDE)
Dosage Form : TABLET
Brand Name : SUNOSI
Dosage Strength : 150MG
Packaging :
Approval Date :
Application Number : 2515822
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : SUNOSI
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 2019-06-17
Application Number : 211230
Regulatory Info : RX
Registration Country : USA

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.
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : SUNOSI
Dosage Strength : EQ 150MG BASE
Packaging :
Approval Date : 2019-06-17
Application Number : 211230
Regulatory Info : RX
Registration Country : USA

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