Purple Biotech
FDA Approved Drugs

Purple Biotech

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 3
  • Latest Approval Date May 31, 2018
  • Data Source FDA
  • First Approval Date May 31, 2018
Company Overview

Company

Purple Biotech

Country

Israel

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Company Snapshot

Purple Biotech

4 Oppenheimer St. Science Park, Rehovot

Israel

purple-biotech.com/ ir@purple-biotech.com View on Map
FDA Approved Drug Records ( 3 records )
2018
31 May
Discontinued Application: 210045

Drug Name

CONSENSI

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE;200MG

Approval Date

2018-05-31

210045 / 1

Active Ingredient

AMLODIPINE BESYLATE; CELECOXIB

Application Number

210045

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE;200MG

Approval Date

2018-05-31

Regulatory Status

Discontinued

2018
31 May
Discontinued Application: 210045

Drug Name

CONSENSI

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE;200MG

Approval Date

2018-05-31

210045 / 2

Active Ingredient

AMLODIPINE BESYLATE; CELECOXIB

Application Number

210045

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE;200MG

Approval Date

2018-05-31

Regulatory Status

Discontinued

2018
31 May
Discontinued Application: 210045

Drug Name

CONSENSI

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE;200MG

Approval Date

2018-05-31

210045 / 3

Active Ingredient

AMLODIPINE BESYLATE; CELECOXIB

Application Number

210045

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE;200MG

Approval Date

2018-05-31

Regulatory Status

Discontinued

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Drug Status Breakdown
3 total
  • 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

CONSENSI

Application Number

210045

Product Number

1

Active Ingredient

AMLODIPINE BESYLATE; CELECOXIB

Dosage Form

-

Strength

EQ 2.5MG BASE;200MG

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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