Dexcel Pharma OTC
FDA Approved Drugs

Dexcel Pharma OTC

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.

OTC
  • Total Records 4
  • Latest Approval Date May 24, 2022
  • Data Source FDA
  • First Approval Date Dec 04, 2007
All
16
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Discontinued
3
View
OTC
4
View
RX
9
View
Company Overview

Company

Dexcel Pharma OTC

Country

Israel

Social Profiles

Company Snapshot

Dexcel Pharma OTC

1 Dexcel St., Or Akiva, 3060000

Israel

dexcel.com/ info@dexcel.com View on Map
FDA Approved Drug Records ( 4 records )
2016
07 Jun
OTC Application: 208025

Drug Name

LANSOPRAZOLE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2016-06-07

208025 / 1

Active Ingredient

LANSOPRAZOLE

Application Number

208025

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2016-06-07

Regulatory Status

OTC

2007
04 Dec
OTC Application: 22032

Drug Name

OMEPRAZOLE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2007-12-04

22032 / 1

Active Ingredient

OMEPRAZOLE

Application Number

22032

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2007-12-04

Regulatory Status

OTC

2017
05 Jul
OTC Application: 209400

Drug Name

OMEPRAZOLE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2017-07-05

209400 / 1

Active Ingredient

OMEPRAZOLE

Application Number

209400

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2017-07-05

Regulatory Status

OTC

2022
24 May
OTC Application: 216096

Drug Name

OMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2022-05-24

216096 / 1

Active Ingredient

OMEPRAZOLE MAGNESIUM

Application Number

216096

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2022-05-24

Regulatory Status

OTC

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Drug Status Breakdown
4 total
  • OTC
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

LANSOPRAZOLE

Application Number

208025

Product Number

1

Active Ingredient

LANSOPRAZOLE

Dosage Form

-

Strength

15MG

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