Hisamitsu Pharmaceutical Co., Inc.
FDA Approved Drugs

Hisamitsu Pharmaceutical Co., Inc.

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.

OTC RX
  • Total Records 5
  • Latest Approval Date Oct 11, 2019
  • Data Source FDA
  • First Approval Date Feb 20, 2008
All
5
View
OTC
2
View
RX
3
View
Company Overview

Company

Hisamitsu Pharmaceutical Co., Inc.

Country

Japan

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Company Snapshot

Hisamitsu Pharmaceutical Co., Inc.

Kyushu Head Office (Registered head office) Saga, Tosu, Tashirodaikan-machi 408, Japan 841-0017

Japan

www.hisamitsu.co.jp/english/ View on Map
FDA Approved Drug Records ( 5 records )
2008
20 Feb
OTC Application: 22029

Drug Name

SALONPAS

Product Number

1

Dosage Form

-

Strength

3%;10%

Approval Date

2008-02-20

22029 / 1

Active Ingredient

MENTHOL; METHYL SALICYLATE

Application Number

22029

Product Number

1

Dosage Form

-

Strength

3%;10%

Approval Date

2008-02-20

Regulatory Status

OTC

2012
05 Nov
OTC Application: 22029

Drug Name

SALONPAS

Product Number

2

Dosage Form

-

Strength

3%;10%

Approval Date

2012-11-05

22029 / 2

Active Ingredient

MENTHOL; METHYL SALICYLATE

Application Number

22029

Product Number

2

Dosage Form

-

Strength

3%;10%

Approval Date

2012-11-05

Regulatory Status

OTC

2019
11 Oct
RX Application: 212268

Drug Name

SECUADO

Product Number

1

Dosage Form

-

Strength

3.8MG/24HR

Approval Date

2019-10-11

212268 / 1

Active Ingredient

ASENAPINE

Application Number

212268

Product Number

1

Dosage Form

-

Strength

3.8MG/24HR

Approval Date

2019-10-11

Regulatory Status

RX

2019
11 Oct
RX Application: 212268

Drug Name

SECUADO

Product Number

2

Dosage Form

-

Strength

5.7MG/24HR

Approval Date

2019-10-11

212268 / 2

Active Ingredient

ASENAPINE

Application Number

212268

Product Number

2

Dosage Form

-

Strength

5.7MG/24HR

Approval Date

2019-10-11

Regulatory Status

RX

2019
11 Oct
RX Application: 212268

Drug Name

SECUADO

Product Number

3

Dosage Form

-

Strength

7.6MG/24HR

Approval Date

2019-10-11

212268 / 3

Active Ingredient

ASENAPINE

Application Number

212268

Product Number

3

Dosage Form

-

Strength

7.6MG/24HR

Approval Date

2019-10-11

Regulatory Status

RX

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Drug Status Breakdown
5 total
  • OTC
  • 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

SALONPAS

Application Number

22029

Product Number

1

Active Ingredient

MENTHOL; METHYL SALICYLATE

Dosage Form

-

Strength

3%;10%

FDA Approved Drug Data

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