Beximco Pharmaceuticals
FDA Approved Drugs

Beximco Pharmaceuticals

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 5
  • Latest Approval Date Aug 12, 2014
  • Data Source FDA
  • First Approval Date Jun 28, 1991
Company Overview

Company

Beximco Pharmaceuticals

Country

Bangladesh

Website

Visit Website

Email

info@bpl.net

Social Profiles

Company Snapshot

Beximco Pharmaceuticals

19 Dhanmondi R/ARoad No. 7Dhaka 1205Bangladesh.

Bangladesh

www.beximco-pharma.com/ info@bpl.net View on Map
FDA Approved Drug Records ( 5 records )
1991
28 Jun
Discontinued Application: 81127

Drug Name

HYDROXYZINE PAMOATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1991-06-28

81127 / 1

Active Ingredient

HYDROXYZINE PAMOATE

Application Number

81127

Product Number

1

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

Approval Date

1991-06-28

Regulatory Status

Discontinued

2014
12 Aug
Discontinued Application: 202546

Drug Name

RIBAVIRIN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2014-08-12

202546 / 1

Active Ingredient

RIBAVIRIN

Application Number

202546

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2014-08-12

Regulatory Status

Discontinued

2014
12 Aug
Discontinued Application: 202546

Drug Name

RIBAVIRIN

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2014-08-12

202546 / 2

Active Ingredient

RIBAVIRIN

Application Number

202546

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2014-08-12

Regulatory Status

Discontinued

2014
12 Aug
Discontinued Application: 202546

Drug Name

RIBAVIRIN

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

2014-08-12

202546 / 3

Active Ingredient

RIBAVIRIN

Application Number

202546

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

2014-08-12

Regulatory Status

Discontinued

2014
12 Aug
Discontinued Application: 202546

Drug Name

RIBAVIRIN

Product Number

4

Dosage Form

-

Strength

600MG

Approval Date

2014-08-12

202546 / 4

Active Ingredient

RIBAVIRIN

Application Number

202546

Product Number

4

Dosage Form

-

Strength

600MG

Approval Date

2014-08-12

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
    5 View
Drug Status Breakdown
5 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

HYDROXYZINE PAMOATE

Application Number

81127

Product Number

1

Active Ingredient

HYDROXYZINE PAMOATE

Dosage Form

-

Strength

EQ 25MG HYDROCHLORIDE

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.
Login to Submit