LNK OTC
FDA Approved Drugs

LNK OTC

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
  • Total Records 4
  • Latest Approval Date Aug 27, 2004
  • Data Source FDA
  • First Approval Date Mar 01, 1999
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8
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Discontinued
4
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OTC
4
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Company

LNK OTC

Country

U.S.A

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LNK OTC

LNK International Inc.

U.S.A

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FDA Approved Drug Records ( 4 records )
2004
27 Aug
OTC Application: 40564

Drug Name

DOXYLAMINE SUCCINATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2004-08-27

40564 / 1

Active Ingredient

DOXYLAMINE SUCCINATE

Application Number

40564

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2004-08-27

Regulatory Status

OTC

1999
01 Mar
OTC Application: 75010

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1999-03-01

75010 / 1

Active Ingredient

IBUPROFEN

Application Number

75010

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1999-03-01

Regulatory Status

OTC

1999
01 Mar
OTC Application: 75139

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1999-03-01

75139 / 1

Active Ingredient

IBUPROFEN

Application Number

75139

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1999-03-01

Regulatory Status

OTC

2003
10 Jun
OTC Application: 76497

Drug Name

LOPERAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2003-06-10

76497 / 1

Active Ingredient

LOPERAMIDE HYDROCHLORIDE

Application Number

76497

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2003-06-10

Regulatory Status

OTC

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Drug Status Breakdown
4 total
  • 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

DOXYLAMINE SUCCINATE

Application Number

40564

Product Number

1

Active Ingredient

DOXYLAMINE SUCCINATE

Dosage Form

-

Strength

25MG

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