Ethypharm RX
FDA Approved Drugs

Ethypharm 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 6
  • Latest Approval Date Mar 31, 2021
  • Data Source FDA
  • First Approval Date Sep 24, 2010
All
8
View
Discontinued
2
View
RX
6
View
Company Overview

Company

Ethypharm RX

Country

France

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Ethypharm RX

194 Bureaux de la Colline, Batiment D – 12eme etage, 92213 Saint-Cloud Cedex

France

www.ethypharm.com/ info@ethypharm.com View on Map
FDA Approved Drug Records ( 6 records )
2010
24 Sep
RX Application: 90622

Drug Name

BUPRENORPHINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2010-09-24

90622 / 1

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE

Application Number

90622

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2010-09-24

Regulatory Status

RX

2010
24 Sep
RX Application: 90622

Drug Name

BUPRENORPHINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2010-09-24

90622 / 2

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE

Application Number

90622

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2010-09-24

Regulatory Status

RX

2015
16 Oct
RX Application: 204431

Drug Name

BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE;EQ 0.5MG BASE

Approval Date

2015-10-16

204431 / 1

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

Application Number

204431

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE;EQ 0.5MG BASE

Approval Date

2015-10-16

Regulatory Status

RX

2015
16 Oct
RX Application: 204431

Drug Name

BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE;EQ 2MG BASE

Approval Date

2015-10-16

204431 / 2

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

Application Number

204431

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE;EQ 2MG BASE

Approval Date

2015-10-16

Regulatory Status

RX

2021
31 Mar
RX Application: 90841

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2021-03-31

90841 / 1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

90841

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2021-03-31

Regulatory Status

RX

2021
31 Mar
RX Application: 90841

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2021-03-31

90841 / 2

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

90841

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2021-03-31

Regulatory Status

RX

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Drug Status Breakdown
6 total
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

BUPRENORPHINE HYDROCHLORIDE

Application Number

90622

Product Number

1

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 2MG BASE

FDA Approved Drug Data

Approved drug product information

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