PLIVA LACHEMA Discontinued
FDA Approved Drugs

PLIVA LACHEMA Discontinued

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 Dec 02, 2008
  • Data Source FDA
  • First Approval Date Mar 12, 2008
All
8
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Unclassified
1
View
Discontinued
7
View
Company Overview

Company

PLIVA LACHEMA Discontinued

Country

Croatia

Social Profiles

Company Snapshot

PLIVA LACHEMA Discontinued

PLIVA HRVATSKA d.o.o. Prilaz baruna Filipovića 25 10000 Zagreb

Croatia

www.pliva.com/ info@pliva.hr View on Map
FDA Approved Drug Records ( 7 records )
2008
02 Dec
Discontinued Application: 78631

Drug Name

CARBOPLATIN

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2008-12-02

78631 / 1

Active Ingredient

CARBOPLATIN

Application Number

78631

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2008-12-02

Regulatory Status

Discontinued

2008
02 Dec
Discontinued Application: 78631

Drug Name

CARBOPLATIN

Product Number

2

Dosage Form

-

Strength

150MG/15ML (10MG/ML)

Approval Date

2008-12-02

78631 / 2

Active Ingredient

CARBOPLATIN

Application Number

78631

Product Number

2

Dosage Form

-

Strength

150MG/15ML (10MG/ML)

Approval Date

2008-12-02

Regulatory Status

Discontinued

2008
02 Dec
Discontinued Application: 78631

Drug Name

CARBOPLATIN

Product Number

3

Dosage Form

-

Strength

450MG/45ML (10MG/ML)

Approval Date

2008-12-02

78631 / 3

Active Ingredient

CARBOPLATIN

Application Number

78631

Product Number

3

Dosage Form

-

Strength

450MG/45ML (10MG/ML)

Approval Date

2008-12-02

Regulatory Status

Discontinued

2008
02 Dec
Discontinued Application: 78631

Drug Name

CARBOPLATIN

Product Number

4

Dosage Form

-

Strength

600MG/60ML (10MG/ML)

Approval Date

2008-12-02

78631 / 4

Active Ingredient

CARBOPLATIN

Application Number

78631

Product Number

4

Dosage Form

-

Strength

600MG/60ML (10MG/ML)

Approval Date

2008-12-02

Regulatory Status

Discontinued

2008
31 Oct
Discontinued Application: 78122

Drug Name

IRINOTECAN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

40MG/2ML (20MG/ML)

Approval Date

2008-10-31

78122 / 1

Active Ingredient

IRINOTECAN HYDROCHLORIDE

Application Number

78122

Product Number

1

Dosage Form

-

Strength

40MG/2ML (20MG/ML)

Approval Date

2008-10-31

Regulatory Status

Discontinued

2008
31 Oct
Discontinued Application: 78122

Drug Name

IRINOTECAN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

100MG/5ML (20MG/ML)

Approval Date

2008-10-31

78122 / 2

Active Ingredient

IRINOTECAN HYDROCHLORIDE

Application Number

78122

Product Number

2

Dosage Form

-

Strength

100MG/5ML (20MG/ML)

Approval Date

2008-10-31

Regulatory Status

Discontinued

2008
12 Mar
Discontinued Application: 77413

Drug Name

PACLITAXEL

Product Number

1

Dosage Form

-

Strength

6MG/ML

Approval Date

2008-03-12

77413 / 1

Active Ingredient

PACLITAXEL

Application Number

77413

Product Number

1

Dosage Form

-

Strength

6MG/ML

Approval Date

2008-03-12

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

CARBOPLATIN

Application Number

78631

Product Number

1

Active Ingredient

CARBOPLATIN

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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