Pharmachemie B.V. RX
FDA Approved Drugs

Pharmachemie B.V. RX

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.

RX
  • Total Records 9
  • Latest Approval Date Feb 27, 2012
  • Data Source FDA
  • First Approval Date May 16, 2000
All
23
View
Discontinued
14
View
RX
9
View
Company Overview

Company

Pharmachemie B.V. RX

Country

Netherlands

Website

Visit Website

Email

pch.servicedesk@tevanederland.com

Social Profiles

Company Snapshot

Pharmachemie B.V. RX

Swensweg 5. P.O. Box 552. 2003 RN Haarlem

Netherlands

www.tevapharmachemie.com/ pch.servicedesk@tevanederland.com View on Map
FDA Approved Drug Records ( 9 records )
2004
14 Oct
RX Application: 77269

Drug Name

CARBOPLATIN

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2004-10-14

77269 / 1

Active Ingredient

CARBOPLATIN

Application Number

77269

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2004-10-14

Regulatory Status

RX

2004
14 Oct
RX Application: 77269

Drug Name

CARBOPLATIN

Product Number

2

Dosage Form

-

Strength

150MG/15ML (10MG/ML)

Approval Date

2004-10-14

77269 / 2

Active Ingredient

CARBOPLATIN

Application Number

77269

Product Number

2

Dosage Form

-

Strength

150MG/15ML (10MG/ML)

Approval Date

2004-10-14

Regulatory Status

RX

2004
14 Oct
RX Application: 77269

Drug Name

CARBOPLATIN

Product Number

3

Dosage Form

-

Strength

450MG/45ML (10MG/ML)

Approval Date

2004-10-14

77269 / 3

Active Ingredient

CARBOPLATIN

Application Number

77269

Product Number

3

Dosage Form

-

Strength

450MG/45ML (10MG/ML)

Approval Date

2004-10-14

Regulatory Status

RX

2007
28 Dec
RX Application: 77269

Drug Name

CARBOPLATIN

Product Number

4

Dosage Form

-

Strength

600MG/60ML (10MG/ML)

Approval Date

2007-12-28

77269 / 4

Active Ingredient

CARBOPLATIN

Application Number

77269

Product Number

4

Dosage Form

-

Strength

600MG/60ML (10MG/ML)

Approval Date

2007-12-28

Regulatory Status

RX

2000
16 May
RX Application: 74656

Drug Name

CISPLATIN

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2000-05-16

74656 / 1

Active Ingredient

CISPLATIN

Application Number

74656

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2000-05-16

Regulatory Status

RX

2010
11 Jan
RX Application: 40843

Drug Name

METHOTREXATE SODIUM PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/40ML (EQ 25MG BASE/ML)

Approval Date

2010-01-11

40843 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

40843

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/40ML (EQ 25MG BASE/ML)

Approval Date

2010-01-11

Regulatory Status

RX

2010
11 Jan
RX Application: 40843

Drug Name

METHOTREXATE SODIUM PRESERVATIVE FREE

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE/2ML (EQ 25MG BASE/ML)

Approval Date

2010-01-11

40843 / 2

Active Ingredient

METHOTREXATE SODIUM

Application Number

40843

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE/2ML (EQ 25MG BASE/ML)

Approval Date

2010-01-11

Regulatory Status

RX

2012
27 Feb
RX Application: 40843

Drug Name

METHOTREXATE SODIUM PRESERVATIVE FREE

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE/4ML (EQ 25MG BASE/ML)

Approval Date

2012-02-27

40843 / 3

Active Ingredient

METHOTREXATE SODIUM

Application Number

40843

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE/4ML (EQ 25MG BASE/ML)

Approval Date

2012-02-27

Regulatory Status

RX

2010
11 Jan
RX Application: 40843

Drug Name

METHOTREXATE SODIUM PRESERVATIVE FREE

Product Number

4

Dosage Form

-

Strength

EQ 250MG BASE/10ML (EQ 25MG BASE/ML)

Approval Date

2010-01-11

40843 / 4

Active Ingredient

METHOTREXATE SODIUM

Application Number

40843

Product Number

4

Dosage Form

-

Strength

EQ 250MG BASE/10ML (EQ 25MG BASE/ML)

Approval Date

2010-01-11

Regulatory Status

RX

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Drug Status Breakdown
9 total
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

CARBOPLATIN

Application Number

77269

Product Number

1

Active Ingredient

CARBOPLATIN

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

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