Axsome Therapeutics
FDA Approved Drugs

Axsome Therapeutics

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

RX
  • Total Records 2
  • Latest Approval Date Jun 17, 2019
  • Data Source FDA
  • First Approval Date Jun 17, 2019
Company Overview

Company

Axsome Therapeutics

Country

U.S.A

Social Profiles

LinkedIn
Company Snapshot

Axsome Therapeutics

200 Broadway, 3rd Floor New York, NY 10038

U.S.A

www.axsome.com/ info@axsome.com View on Map
FDA Approved Drug Records ( 2 records )
2019
17 Jun
RX Application: 211230

Drug Name

SUNOSI

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2019-06-17

211230 / 1

Active Ingredient

SOLRIAMFETOL HYDROCHLORIDE

Application Number

211230

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2019-06-17

Regulatory Status

RX

2019
17 Jun
RX Application: 211230

Drug Name

SUNOSI

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2019-06-17

211230 / 2

Active Ingredient

SOLRIAMFETOL HYDROCHLORIDE

Application Number

211230

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2019-06-17

Regulatory Status

RX

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Drug Status Breakdown
2 total
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

SUNOSI

Application Number

211230

Product Number

1

Active Ingredient

SOLRIAMFETOL HYDROCHLORIDE

Dosage Form

-

Strength

EQ 75MG BASE

FDA Approved Drug Data

Approved drug product information

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