Somerset Pharmaceuticals Inc OTC
FDA Approved Drugs

Somerset Pharmaceuticals Inc 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 1
  • Latest Approval Date Dec 18, 2024
  • Data Source FDA
  • First Approval Date Dec 18, 2024
All
29
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Unclassified
3
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OTC
1
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RX
25
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Company Overview

Company

Somerset Pharmaceuticals Inc OTC

Country

U.S.A

Social Profiles

Company Snapshot

Somerset Pharmaceuticals Inc OTC

5215 W. Laurel St. Tampa, FL 33607

U.S.A

www.somersetpharm.com/ mlg@somersetpharm.com View on Map
FDA Approved Drug Records ( 1 record )
2024
18 Dec
OTC Application: 215006

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2024-12-18

215006 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

215006

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2024-12-18

Regulatory Status

OTC

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Drug Status Breakdown
1 total
  • OTC
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

OLOPATADINE HYDROCHLORIDE

Application Number

215006

Product Number

1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 0.2% BASE

FDA Approved Drug Data

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