GLAND PHARMA LIMITED
NDC Database

GLAND PHARMA LIMITED

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 3
  • Latest Marketing Date 2026-01-06
  • Data Source FDA
  • First Marketing Date 2020-08-20
Company Overview

Company

GLAND PHARMA LIMITED

Country

India

Social Profiles

Company Snapshot

GLAND PHARMA LIMITED

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

India

glandpharma.com/ gland@glandpharma.com View on Map
NDC Records ( 3 records )
2020
20 Aug
Bulk Ingredient NDC: 68083-231

Nonproprietary Name

Olopatadine Hydrochloride Ophthalmic

Dosage Form

SOLUTION

Strength

2 mg/mL

Labeler

Gland Pharma Limited

Marketing Category

EXPORT ONLY

68083-231

Substance

OLOPATADINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-08-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
06 Jan
Bulk Ingredient NDC: 68083-398

Nonproprietary Name

olopatadine hydrochloride ophthalmic

Dosage Form

SOLUTION

Strength

7 mg/mL

Labeler

Gland Pharma Limited

Marketing Category

EXPORT ONLY

68083-398

Substance

OLOPATADINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-01-06

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2020
01 Sep
Bulk Ingredient NDC: 68083-477

Nonproprietary Name

olopatadine hydrochloride ophthalmic

Dosage Form

SOLUTION/ DROPS

Strength

1 mg/mL

Labeler

Gland Pharma Limited

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

68083-477

Substance

OLOPATADINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
3 total
  • Bulk Ingredient
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

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NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

68083-231

Nonproprietary Name

Olopatadine Hydrochloride Ophthalmic

Labeler

Gland Pharma Limited

Dosage Form

SOLUTION

FDA NDC Data

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Data maintained from official sources

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Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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