Unichem Laboratories Limited Unclassified
FDA Approved Drugs

Unichem 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 7
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
20
View
Unclassified
7
View
RX
13
View
Company Overview

Company

Unichem Laboratories Limited Unclassified

Country

India

Social Profiles

LinkedIn
Company Snapshot

Unichem Laboratories Limited Unclassified

Unichem Bhavan Prabhat Estate, Off S.V.Road, Jogeshwari (West), Mumbai - 400 102

India

www.unichemlabs.com/ unichemindia@mail.ru View on Map
FDA Approved Drug Records ( 7 records )
-
Unclassified Application: 210108

Drug Name

APIXABAN

Product Number

2

Dosage Form

-

Strength

1.5MG

Approval Date

-

210108 / 2

Active Ingredient

APIXABAN

Application Number

210108

Product Number

2

Dosage Form

-

Strength

1.5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 210108

Drug Name

APIXABAN

Product Number

3

Dosage Form

-

Strength

2.0MG

Approval Date

-

210108 / 3

Active Ingredient

APIXABAN

Application Number

210108

Product Number

3

Dosage Form

-

Strength

2.0MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 210108

Drug Name

APIXABAN

Product Number

4

Dosage Form

-

Strength

5MG

Approval Date

-

210108 / 4

Active Ingredient

APIXABAN

Application Number

210108

Product Number

4

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 210108

Drug Name

APIXABAN

Product Number

5

Dosage Form

-

Strength

2.5MG

Approval Date

-

210108 / 5

Active Ingredient

APIXABAN

Application Number

210108

Product Number

5

Dosage Form

-

Strength

2.5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214693

Drug Name

SITAGLIPTIN PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

-

214693 / 1

Active Ingredient

SITAGLIPTIN PHOSPHATE

Application Number

214693

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214693

Drug Name

SITAGLIPTIN PHOSPHATE

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

-

214693 / 2

Active Ingredient

SITAGLIPTIN PHOSPHATE

Application Number

214693

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214693

Drug Name

SITAGLIPTIN PHOSPHATE

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

-

214693 / 3

Active Ingredient

SITAGLIPTIN PHOSPHATE

Application Number

214693

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
7 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

APIXABAN

Application Number

210108

Product Number

2

Active Ingredient

APIXABAN

Dosage Form

-

Strength

1.5MG

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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