Tonix Pharmaceuticals Holding Corp
FDA Approved Drugs

Tonix Pharmaceuticals Holding Corp

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 Jan 25, 2019
  • Data Source FDA
  • First Approval Date Jan 28, 2016
Company Overview

Company

Tonix Pharmaceuticals Holding Corp

Country

U.S.A

Email

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Company Snapshot

Tonix Pharmaceuticals Holding Corp

509 Madison Avenue Suite 306 New York, NY 10022

U.S.A

www.tonixpharma.com/ View on Map
FDA Approved Drug Records ( 2 records )
2019
25 Jan
RX Application: 210884

Drug Name

TOSYMRA

Product Number

1

Dosage Form

-

Strength

10MG/SPRAY

Approval Date

2019-01-25

210884 / 1

Active Ingredient

SUMATRIPTAN

Application Number

210884

Product Number

1

Dosage Form

-

Strength

10MG/SPRAY

Approval Date

2019-01-25

Regulatory Status

RX

2016
28 Jan
RX Application: 208223

Drug Name

ZEMBRACE SYMTOUCH

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/0.5ML (EQ 3MG BASE/0.5ML)

Approval Date

2016-01-28

208223 / 1

Active Ingredient

SUMATRIPTAN SUCCINATE

Application Number

208223

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/0.5ML (EQ 3MG BASE/0.5ML)

Approval Date

2016-01-28

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

TOSYMRA

Application Number

210884

Product Number

1

Active Ingredient

SUMATRIPTAN

Dosage Form

-

Strength

10MG/SPRAY

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