Sovereign Pharmaceuticals, LLC
FDA Approved Drugs

Sovereign Pharmaceuticals, LLC

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 4
  • Latest Approval Date Jul 23, 2015
  • Data Source FDA
  • First Approval Date Nov 14, 2014
Company Overview

Company

Sovereign Pharmaceuticals, LLC

Country

U.S.A

Website

Visit Website

Email

jhunter@sovpharm.com.

Social Profiles

Company Snapshot

Sovereign Pharmaceuticals, LLC

Riverbend Business Park, Building # 15, 7590 Sand St., Ft. Worth, TX 76118, USA

U.S.A

www.sovpharm.com/ jhunter@sovpharm.com. View on Map
FDA Approved Drug Records ( 4 records )
2015
23 Jul
Discontinued Application: 204900

Drug Name

AMLODIPINE BESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2015-07-23

204900 / 1

Active Ingredient

AMLODIPINE BESYLATE

Application Number

204900

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2015-07-23

Regulatory Status

Discontinued

2015
23 Jul
Discontinued Application: 204900

Drug Name

AMLODIPINE BESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2015-07-23

204900 / 2

Active Ingredient

AMLODIPINE BESYLATE

Application Number

204900

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2015-07-23

Regulatory Status

Discontinued

2015
23 Jul
Discontinued Application: 204900

Drug Name

AMLODIPINE BESYLATE

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-07-23

204900 / 3

Active Ingredient

AMLODIPINE BESYLATE

Application Number

204900

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-07-23

Regulatory Status

Discontinued

2014
14 Nov
Discontinued Application: 205474

Drug Name

OBREDON

Product Number

1

Dosage Form

-

Strength

200MG/5ML;2.5MG/5ML

Approval Date

2014-11-14

205474 / 1

Active Ingredient

GUAIFENESIN; HYDROCODONE BITARTRATE

Application Number

205474

Product Number

1

Dosage Form

-

Strength

200MG/5ML;2.5MG/5ML

Approval Date

2014-11-14

Regulatory Status

Discontinued

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Drug Status Breakdown
4 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

AMLODIPINE BESYLATE

Application Number

204900

Product Number

1

Active Ingredient

AMLODIPINE BESYLATE

Dosage Form

-

Strength

EQ 2.5MG BASE

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

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