LNK
FDA Approved Drugs

LNK

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 8
  • Latest Approval Date Aug 27, 2004
  • Data Source FDA
  • First Approval Date Jan 27, 1983
All
8
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Discontinued
4
View
OTC
4
View
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Company

LNK

Country

U.S.A

Website

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LNK

LNK International Inc.

U.S.A

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FDA Approved Drug Records ( 8 records )
1983
27 Jan
Discontinued Application: 87977

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-01-27

87977 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

87977

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-01-27

Regulatory Status

Discontinued

1983
27 Jan
Discontinued Application: 87978

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-01-27

87978 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

87978

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-01-27

Regulatory Status

Discontinued

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

2004
17 Jun
Discontinued Application: 76741

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2004-06-17

76741 / 1

Active Ingredient

IBUPROFEN

Application Number

76741

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2004-06-17

Regulatory Status

Discontinued

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

1984
10 Apr
Discontinued Application: 19029

Drug Name

METRONIDAZOLE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1984-04-10

19029 / 1

Active Ingredient

METRONIDAZOLE

Application Number

19029

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1984-04-10

Regulatory Status

Discontinued

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Drug Status Breakdown
8 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

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

87977

Product Number

1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Dosage Form

-

Strength

25MG

FDA Approved Drug Data

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