Alembic Pharmaceuticals Limited Unclassified
FDA Approved Drugs

Alembic Pharmaceuticals 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 10
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
533
View
Unclassified
10
View
Discontinued
28
View
OTC
4
View
RX
491
View
Company Overview

Company

Alembic Pharmaceuticals Limited Unclassified

Country

India

Website

Visit Website

Email

infoal@alembic.co.in

Social Profiles

LinkedIn
Company Snapshot

Alembic Pharmaceuticals Limited Unclassified

Alembic Road, Vadodara - 390 003, Gujarat

India

www.alembic-india.com/ infoal@alembic.co.in View on Map
FDA Approved Drug Records ( 10 records )
-
Unclassified Application: 216775

Drug Name

ACALABRUTINIB

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

216775 / 1

Active Ingredient

ACALABRUTINIB

Application Number

216775

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 217678

Drug Name

BINIMETINIB

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

-

217678 / 1

Active Ingredient

BINIMETINIB

Application Number

217678

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 208046

Drug Name

DABIGATRAN ETEXILATE MESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

-

208046 / 1

Active Ingredient

DABIGATRAN ETEXILATE MESYLATE

Application Number

208046

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 207409

Drug Name

ILOPERIDONE

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

-

207409 / 2

Active Ingredient

ILOPERIDONE

Application Number

207409

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 207409

Drug Name

ILOPERIDONE

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

-

207409 / 3

Active Ingredient

ILOPERIDONE

Application Number

207409

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 207409

Drug Name

ILOPERIDONE

Product Number

4

Dosage Form

-

Strength

6MG

Approval Date

-

207409 / 4

Active Ingredient

ILOPERIDONE

Application Number

207409

Product Number

4

Dosage Form

-

Strength

6MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 207409

Drug Name

ILOPERIDONE

Product Number

5

Dosage Form

-

Strength

8MG

Approval Date

-

207409 / 5

Active Ingredient

ILOPERIDONE

Application Number

207409

Product Number

5

Dosage Form

-

Strength

8MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 207409

Drug Name

ILOPERIDONE

Product Number

6

Dosage Form

-

Strength

10MG

Approval Date

-

207409 / 6

Active Ingredient

ILOPERIDONE

Application Number

207409

Product Number

6

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 220639

Drug Name

LAROTRECTINIB

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

220639 / 1

Active Ingredient

LAROTRECTINIB

Application Number

220639

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 215677

Drug Name

RIBOCICLIB

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

-

215677 / 1

Active Ingredient

RIBOCICLIB

Application Number

215677

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
10 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

ACALABRUTINIB

Application Number

216775

Product Number

1

Active Ingredient

ACALABRUTINIB

Dosage Form

-

Strength

100MG

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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