Eugia Pharma OTC
FDA Approved Drugs

Eugia Pharma 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 2
  • Latest Approval Date Apr 04, 2019
  • Data Source FDA
  • First Approval Date Dec 18, 2015
All
256
View
Unclassified
12
View
Discontinued
71
View
OTC
2
View
RX
171
View
Company Overview

Company

Eugia Pharma OTC

Country

India

Social Profiles

LinkedIn
Company Snapshot

Eugia Pharma OTC

Forming part of Sy No 83/1, Hyderabad Knowledge City TSIIC Raidurg, Panmaktha Plot, 1, Hitech City Rd, opp. IKEA Hyderabad, Telangana 500081

India

www.eugiapharma.com/ info@eugia.co.in View on Map
FDA Approved Drug Records ( 2 records )
2015
18 Dec
OTC Application: 204812

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

2015-12-18

204812 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

204812

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

2015-12-18

Regulatory Status

OTC

2019
04 Apr
OTC Application: 209995

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2019-04-04

209995 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

209995

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2019-04-04

Regulatory Status

OTC

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
    256 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
2 total
  • OTC
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

OLOPATADINE HYDROCHLORIDE

Application Number

204812

Product Number

1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 0.1% BASE

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.