Karo Pharma
FDA Approved Drugs

Karo Pharma

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.

Discontinued OTC
  • Total Records 6
  • Latest Approval Date Jul 24, 2006
  • Data Source FDA
  • First Approval Date Oct 17, 1997
All
6
View
Discontinued
2
View
OTC
4
View
Company Overview

Company

Karo Pharma

Country

Sweden

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Company Snapshot

Karo Pharma

Box 16184 103 24 Stockholm

Sweden

www.karopharma.com/ View on Map
FDA Approved Drug Records ( 6 records )
1997
17 Oct
Discontinued Application: 20749

Drug Name

LAMISIL

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1997-10-17

20749 / 1

Active Ingredient

TERBINAFINE HYDROCHLORIDE

Application Number

20749

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1997-10-17

Regulatory Status

Discontinued

1998
29 Apr
Discontinued Application: 20846

Drug Name

LAMISIL

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1998-04-29

20846 / 1

Active Ingredient

TERBINAFINE

Application Number

20846

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1998-04-29

Regulatory Status

Discontinued

1999
09 Mar
OTC Application: 20980

Drug Name

LAMISIL

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1999-03-09

20980 / 1

Active Ingredient

TERBINAFINE HYDROCHLORIDE

Application Number

20980

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1999-03-09

Regulatory Status

OTC

2000
17 Mar
OTC Application: 21124

Drug Name

LAMISIL AT

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2000-03-17

21124 / 1

Active Ingredient

TERBINAFINE HYDROCHLORIDE

Application Number

21124

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2000-03-17

Regulatory Status

OTC

2000
17 Mar
OTC Application: 21124

Drug Name

LAMISIL AT

Product Number

2

Dosage Form

-

Strength

1%

Approval Date

2000-03-17

21124 / 2

Active Ingredient

TERBINAFINE HYDROCHLORIDE

Application Number

21124

Product Number

2

Dosage Form

-

Strength

1%

Approval Date

2000-03-17

Regulatory Status

OTC

2006
24 Jul
OTC Application: 21958

Drug Name

LAMISIL AT

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2006-07-24

21958 / 1

Active Ingredient

TERBINAFINE

Application Number

21958

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2006-07-24

Regulatory Status

OTC

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Drug Status Breakdown
6 total
  • Discontinued
  • OTC
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

LAMISIL

Application Number

20749

Product Number

1

Active Ingredient

TERBINAFINE HYDROCHLORIDE

Dosage Form

-

Strength

1%

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