Dexcel Pharma RX
FDA Approved Drugs

Dexcel Pharma RX

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
  • Total Records 9
  • Latest Approval Date Apr 02, 2026
  • Data Source FDA
  • First Approval Date Feb 19, 2016
All
16
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Discontinued
3
View
OTC
4
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RX
9
View
Company Overview

Company

Dexcel Pharma RX

Country

Israel

Social Profiles

Company Snapshot

Dexcel Pharma RX

1 Dexcel St., Or Akiva, 3060000

Israel

dexcel.com/ info@dexcel.com View on Map
FDA Approved Drug Records ( 9 records )
2016
19 Feb
RX Application: 203713

Drug Name

DONEPEZIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

23MG

Approval Date

2016-02-19

203713 / 1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

203713

Product Number

1

Dosage Form

-

Strength

23MG

Approval Date

2016-02-19

Regulatory Status

RX

2019
03 Oct
RX Application: 211379

Drug Name

HEMADY

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2019-10-03

211379 / 1

Active Ingredient

DEXAMETHASONE

Application Number

211379

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2019-10-03

Regulatory Status

RX

2026
02 Apr
RX Application: 219819

Drug Name

NINTEDANIB ESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2026-04-02

219819 / 1

Active Ingredient

NINTEDANIB ESYLATE

Application Number

219819

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2026-04-02

Regulatory Status

RX

2026
02 Apr
RX Application: 219819

Drug Name

NINTEDANIB ESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2026-04-02

219819 / 2

Active Ingredient

NINTEDANIB ESYLATE

Application Number

219819

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2026-04-02

Regulatory Status

RX

2023
16 Jun
RX Application: 216247

Drug Name

PANTOPRAZOLE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2023-06-16

216247 / 1

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

216247

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2023-06-16

Regulatory Status

RX

2024
16 Dec
RX Application: 218668

Drug Name

TOFACITINIB CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 11MG BASE

Approval Date

2024-12-16

218668 / 1

Active Ingredient

TOFACITINIB CITRATE

Application Number

218668

Product Number

1

Dosage Form

-

Strength

EQ 11MG BASE

Approval Date

2024-12-16

Regulatory Status

RX

2019
31 Oct
RX Application: 209193

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2019-10-31

209193 / 1

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

209193

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2019-10-31

Regulatory Status

RX

2019
31 Oct
RX Application: 209193

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 225MG BASE

Approval Date

2019-10-31

209193 / 2

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

209193

Product Number

2

Dosage Form

-

Strength

EQ 225MG BASE

Approval Date

2019-10-31

Regulatory Status

RX

2021
23 Sep
RX Application: 215109

Drug Name

VIGABATRIN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2021-09-23

215109 / 1

Active Ingredient

VIGABATRIN

Application Number

215109

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2021-09-23

Regulatory Status

RX

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Drug Status Breakdown
9 total
  • RX
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

DONEPEZIL HYDROCHLORIDE

Application Number

203713

Product Number

1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Dosage Form

-

Strength

23MG

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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