Chemi SpA
FDA Approved Drugs

Chemi 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 Discontinued
  • Total Records 10
  • Latest Approval Date May 07, 2025
  • Data Source FDA
  • First Approval Date Sep 02, 2014
All
10
View
Discontinued
1
View
RX
9
View
Company Overview

Company

Chemi SpA

Country

Italy

Website

Visit Website

Email

chemi@chemi.com

Social Profiles

LinkedIn
Company Snapshot

Chemi SpA

Via dei lavoratori 54, 20092 Cinisello Balsamo (Milano)

Italy

www.chemi.com/ chemi@chemi.com View on Map
FDA Approved Drug Records ( 10 records )
2017
22 Sep
RX Application: 206033

Drug Name

DECITABINE

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2017-09-22

206033 / 1

Active Ingredient

DECITABINE

Application Number

206033

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2017-09-22

Regulatory Status

RX

2025
07 May
RX Application: 208468

Drug Name

GLATIRAMER ACETATE

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2025-05-07

208468 / 1

Active Ingredient

GLATIRAMER ACETATE

Application Number

208468

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2025-05-07

Regulatory Status

RX

2025
07 May
RX Application: 208468

Drug Name

GLATIRAMER ACETATE

Product Number

2

Dosage Form

-

Strength

40MG/ML

Approval Date

2025-05-07

208468 / 2

Active Ingredient

GLATIRAMER ACETATE

Application Number

208468

Product Number

2

Dosage Form

-

Strength

40MG/ML

Approval Date

2025-05-07

Regulatory Status

RX

2014
02 Sep
Discontinued Application: 202235

Drug Name

IBANDRONATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/3ML

Approval Date

2014-09-02

202235 / 1

Active Ingredient

IBANDRONATE SODIUM

Application Number

202235

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/3ML

Approval Date

2014-09-02

Regulatory Status

Discontinued

2016
23 Nov
RX Application: 204639

Drug Name

TEMOZOLOMIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2016-11-23

204639 / 1

Active Ingredient

TEMOZOLOMIDE

Application Number

204639

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2016-11-23

Regulatory Status

RX

2016
23 Nov
RX Application: 204639

Drug Name

TEMOZOLOMIDE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2016-11-23

204639 / 2

Active Ingredient

TEMOZOLOMIDE

Application Number

204639

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2016-11-23

Regulatory Status

RX

2016
23 Nov
RX Application: 204639

Drug Name

TEMOZOLOMIDE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2016-11-23

204639 / 3

Active Ingredient

TEMOZOLOMIDE

Application Number

204639

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2016-11-23

Regulatory Status

RX

2016
23 Nov
RX Application: 204639

Drug Name

TEMOZOLOMIDE

Product Number

4

Dosage Form

-

Strength

140MG

Approval Date

2016-11-23

204639 / 4

Active Ingredient

TEMOZOLOMIDE

Application Number

204639

Product Number

4

Dosage Form

-

Strength

140MG

Approval Date

2016-11-23

Regulatory Status

RX

2016
23 Nov
RX Application: 204639

Drug Name

TEMOZOLOMIDE

Product Number

5

Dosage Form

-

Strength

180MG

Approval Date

2016-11-23

204639 / 5

Active Ingredient

TEMOZOLOMIDE

Application Number

204639

Product Number

5

Dosage Form

-

Strength

180MG

Approval Date

2016-11-23

Regulatory Status

RX

2016
23 Nov
RX Application: 204639

Drug Name

TEMOZOLOMIDE

Product Number

6

Dosage Form

-

Strength

250MG

Approval Date

2016-11-23

204639 / 6

Active Ingredient

TEMOZOLOMIDE

Application Number

204639

Product Number

6

Dosage Form

-

Strength

250MG

Approval Date

2016-11-23

Regulatory Status

RX

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Drug Status Breakdown
10 total
  • RX
  • Discontinued
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

DECITABINE

Application Number

206033

Product Number

1

Active Ingredient

DECITABINE

Dosage Form

-

Strength

50MG/VIAL

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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