Opocrin SpA
FDA Approved Drugs

Opocrin SpA

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 Unclassified
  • Total Records 6
  • Latest Approval Date Sep 29, 2014
  • Data Source FDA
  • First Approval Date Feb 04, 1999
All
6
View
Unclassified
1
View
RX
5
View
Company Overview

Company

Opocrin SpA

Country

Italy

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Company Snapshot
FDA Approved Drug Records ( 6 records )
2013
28 Feb
RX Application: 202971

Drug Name

ABILIFY MAINTENA KIT

Product Number

1

Dosage Form

-

Strength

300MG/VIAL

Approval Date

2013-02-28

202971 / 1

Active Ingredient

ARIPIPRAZOLE

Application Number

202971

Product Number

1

Dosage Form

-

Strength

300MG/VIAL

Approval Date

2013-02-28

Regulatory Status

RX

2013
28 Feb
RX Application: 202971

Drug Name

ABILIFY MAINTENA KIT

Product Number

2

Dosage Form

-

Strength

400MG/VIAL

Approval Date

2013-02-28

202971 / 2

Active Ingredient

ARIPIPRAZOLE

Application Number

202971

Product Number

2

Dosage Form

-

Strength

400MG/VIAL

Approval Date

2013-02-28

Regulatory Status

RX

2014
29 Sep
RX Application: 202971

Drug Name

ABILIFY MAINTENA KIT

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2014-09-29

202971 / 3

Active Ingredient

ARIPIPRAZOLE

Application Number

202971

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2014-09-29

Regulatory Status

RX

2014
29 Sep
RX Application: 202971

Drug Name

ABILIFY MAINTENA KIT

Product Number

4

Dosage Form

-

Strength

400MG

Approval Date

2014-09-29

202971 / 4

Active Ingredient

ARIPIPRAZOLE

Application Number

202971

Product Number

4

Dosage Form

-

Strength

400MG

Approval Date

2014-09-29

Regulatory Status

RX

1999
04 Feb
RX Application: 20954

Drug Name

BUSULFEX

Product Number

1

Dosage Form

-

Strength

6MG/ML

Approval Date

1999-02-04

20954 / 1

Active Ingredient

BUSULFAN

Application Number

20954

Product Number

1

Dosage Form

-

Strength

6MG/ML

Approval Date

1999-02-04

Regulatory Status

RX

-
Unclassified Application: 761434

Drug Name

VOYXACT

Product Number

1

Dosage Form

-

Strength

400MG/2ML(200MG/ML)

Approval Date

-

761434 / 1

Active Ingredient

SIBEPRENLIMAB-SZSI

Application Number

761434

Product Number

1

Dosage Form

-

Strength

400MG/2ML(200MG/ML)

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
6 total
  • RX
  • Unclassified
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

ABILIFY MAINTENA KIT

Application Number

202971

Product Number

1

Active Ingredient

ARIPIPRAZOLE

Dosage Form

-

Strength

300MG/VIAL

FDA Approved Drug Data

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