Dexcel Pharma Discontinued
FDA Approved Drugs

Dexcel Pharma 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 3
  • Latest Approval Date May 13, 2021
  • Data Source FDA
  • First Approval Date May 15, 1998
All
16
View
Discontinued
3
View
OTC
4
View
RX
9
View
Company Overview

Company

Dexcel Pharma Discontinued

Country

Israel

Social Profiles

Company Snapshot

Dexcel Pharma Discontinued

1 Dexcel St., Or Akiva, 3060000

Israel

dexcel.com/ info@dexcel.com View on Map
FDA Approved Drug Records ( 3 records )
2020
20 Oct
Discontinued Application: 214278

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2020-10-20

214278 / 1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

214278

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2020-10-20

Regulatory Status

Discontinued

1998
15 May
Discontinued Application: 20774

Drug Name

PERIOCHIP

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1998-05-15

20774 / 1

Active Ingredient

CHLORHEXIDINE GLUCONATE

Application Number

20774

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

1998-05-15

Regulatory Status

Discontinued

2021
13 May
Discontinued Application: 214992

Drug Name

VIGABATRIN

Product Number

1

Dosage Form

-

Strength

500MG/PACKET

Approval Date

2021-05-13

214992 / 1

Active Ingredient

VIGABATRIN

Application Number

214992

Product Number

1

Dosage Form

-

Strength

500MG/PACKET

Approval Date

2021-05-13

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    16 View
  • Drug Prices in Switzerland
    0 View
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

ESOMEPRAZOLE MAGNESIUM

Application Number

214278

Product Number

1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Dosage Form

-

Strength

EQ 20MG BASE

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

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.