RANBAXY LABORATORIES LIMITED Unclassified
FDA Approved Drugs

RANBAXY LABORATORIES LIMITED Unclassified

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.

Unclassified
  • Total Records 14
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
111
View
Unclassified
14
View
Discontinued
88
View
OTC
4
View
RX
5
View
Company Overview

Company

RANBAXY LABORATORIES LIMITED Unclassified

Country

India

Website

Visit Website

Email

corporate.communications@ranbaxy.com

Social Profiles

Company Snapshot

RANBAXY LABORATORIES LIMITED Unclassified

Plot 90, Sector 32,Gurgaon-122001 (Haryana)

India

ranbaxy.com corporate.communications@ranbaxy.com View on Map
FDA Approved Drug Records ( 14 records )
-
Unclassified Application: 76970

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

-

76970 / 1

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76970

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76970

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

-

76970 / 2

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76970

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76970

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

180MG

Approval Date

-

76970 / 3

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

76970

Product Number

3

Dosage Form

-

Strength

180MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 77588

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

-

77588 / 1

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77588

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 77588

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

8MG

Approval Date

-

77588 / 2

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77588

Product Number

2

Dosage Form

-

Strength

8MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 77588

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

3

Dosage Form

-

Strength

12MG

Approval Date

-

77588 / 3

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77588

Product Number

3

Dosage Form

-

Strength

12MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 77357

Drug Name

LAMIVUDINE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

-

77357 / 1

Active Ingredient

LAMIVUDINE

Application Number

77357

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 202529

Drug Name

LAMIVUDINE; TENOFOVIR DISOPROXIL FUMARATE

Product Number

1

Dosage Form

-

Strength

300MG; 300MG

Approval Date

-

202529 / 1

Active Ingredient

LAMIVUDINE; TENOFOVIR DISOPROXIL FUMARATE

Application Number

202529

Product Number

1

Dosage Form

-

Strength

300MG; 300MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 77429

Drug Name

NEVIRAPINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

-

77429 / 1

Active Ingredient

NEVIRAPINE

Application Number

77429

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 77416

Drug Name

RISPERIDONE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

-

77416 / 1

Active Ingredient

RISPERIDONE

Application Number

77416

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 77363

Drug Name

RIVASTIGMINE

Product Number

1

Dosage Form

-

Strength

2MG/ML

Approval Date

-

77363 / 1

Active Ingredient

RIVASTIGMINE TARTRATE

Application Number

77363

Product Number

1

Dosage Form

-

Strength

2MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 203351

Drug Name

SODIUM OXYBATE

Product Number

1

Dosage Form

-

Strength

500MG/ML

Approval Date

-

203351 / 1

Active Ingredient

SODIUM OXYBATE

Application Number

203351

Product Number

1

Dosage Form

-

Strength

500MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76953

Drug Name

TOLTERODINE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

-

76953 / 1

Active Ingredient

TOLTERODINE TARTRATE

Application Number

76953

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76953

Drug Name

TOLTERODINE

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

-

76953 / 2

Active Ingredient

TOLTERODINE TARTRATE

Application Number

76953

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
14 total
  • Unclassified
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

FEXOFENADINE HYDROCHLORIDE

Application Number

76970

Product Number

1

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Dosage Form

-

Strength

30MG

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

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