GLAND PHARMA LIMITED OTC
FDA Approved Drugs

GLAND PHARMA LIMITED 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 4
  • Latest Approval Date Jan 06, 2026
  • Data Source FDA
  • First Approval Date Aug 02, 2019
All
240
View
Unclassified
10
View
Discontinued
6
View
OTC
4
View
RX
220
View
Company Overview

Company

GLAND PHARMA LIMITED OTC

Country

India

Social Profiles

Company Snapshot

GLAND PHARMA LIMITED OTC

6-3-865/1/2, Greenland Apartments Ameerpet, Hyderabad - 500016

India

glandpharma.com/ gland@glandpharma.com View on Map
FDA Approved Drug Records ( 4 records )
2024
01 Mar
OTC Application: 209706

Drug Name

ALCAFTADINE

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

2024-03-01

209706 / 1

Active Ingredient

ALCAFTADINE

Application Number

209706

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

2024-03-01

Regulatory Status

OTC

2019
02 Aug
OTC Application: 209619

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

2019-08-02

209619 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

209619

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

2019-08-02

Regulatory Status

OTC

2020
20 May
OTC Application: 209752

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2020-05-20

209752 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

209752

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2020-05-20

Regulatory Status

OTC

2026
06 Jan
OTC Application: 213514

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.7% BASE

Approval Date

2026-01-06

213514 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

213514

Product Number

1

Dosage Form

-

Strength

EQ 0.7% BASE

Approval Date

2026-01-06

Regulatory Status

OTC

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Drug Status Breakdown
4 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

ALCAFTADINE

Application Number

209706

Product Number

1

Active Ingredient

ALCAFTADINE

Dosage Form

-

Strength

0.25%

FDA Approved Drug Data

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