West Pharmaceutical Services
FDA Approved Drugs

West Pharmaceutical Services

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
  • Total Records 7
  • Latest Approval Date Aug 25, 1992
  • Data Source FDA
  • First Approval Date Nov 07, 1988
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Company

West Pharmaceutical Services

Country

U.S.A

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Company Snapshot

West Pharmaceutical Services

530 Herman O. West Drive Exton, PA 19341

U.S.A

www.westpharma.com/ View on Map
FDA Approved Drug Records ( 7 records )
1988
07 Nov
Discontinued Application: 62932

Drug Name

GENTAMICIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/ML

Approval Date

1988-11-07

62932 / 1

Active Ingredient

GENTAMICIN SULFATE

Application Number

62932

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/ML

Approval Date

1988-11-07

Regulatory Status

Discontinued

1992
25 Aug
Discontinued Application: 72029

Drug Name

LACTULOSE

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1992-08-25

72029 / 1

Active Ingredient

LACTULOSE

Application Number

72029

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1992-08-25

Regulatory Status

Discontinued

1992
25 Aug
Discontinued Application: 73160

Drug Name

LACTULOSE

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1992-08-25

73160 / 1

Active Ingredient

LACTULOSE

Application Number

73160

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1992-08-25

Regulatory Status

Discontinued

1989
30 Jun
Discontinued Application: 89688

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

1989-06-30

89688 / 1

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

89688

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

1989-06-30

Regulatory Status

Discontinued

1988
05 Dec
Discontinued Application: 71665

Drug Name

METOCLOPRAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

1988-12-05

71665 / 1

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

71665

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

1988-12-05

Regulatory Status

Discontinued

1989
20 Sep
Discontinued Application: 71917

Drug Name

THIOTHIXENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML

Approval Date

1989-09-20

71917 / 1

Active Ingredient

THIOTHIXENE HYDROCHLORIDE

Application Number

71917

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML

Approval Date

1989-09-20

Regulatory Status

Discontinued

1988
16 Dec
Discontinued Application: 71939

Drug Name

THIOTHIXENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

1988-12-16

71939 / 1

Active Ingredient

THIOTHIXENE HYDROCHLORIDE

Application Number

71939

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/ML

Approval Date

1988-12-16

Regulatory Status

Discontinued

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Drug Status Breakdown
7 total
  • Discontinued
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

GENTAMICIN SULFATE

Application Number

62932

Product Number

1

Active Ingredient

GENTAMICIN SULFATE

Dosage Form

-

Strength

EQ 3MG BASE/ML

FDA Approved Drug Data

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