Micro Labs Limited Unclassified
FDA Approved Drugs

Micro Labs 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
214
View
Unclassified
14
View
Discontinued
9
View
RX
191
View
Company Overview

Company

Micro Labs Limited Unclassified

Country

India

Website

Visit Website

Email

Social Profiles

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Company Snapshot

Micro Labs Limited Unclassified

27, RACE COURSE ROAD, BANGALORE-560 001

India

www.microlabsltd.com/ View on Map
FDA Approved Drug Records ( 14 records )
-
Unclassified Application: 204638

Drug Name

BIMATOPROST

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

-

204638 / 1

Active Ingredient

BIMATOPROST

Application Number

204638

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 212179

Drug Name

DOLUTEGRAVIR SODIUM

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

212179 / 1

Active Ingredient

DOLUTEGRAVIR SODIUM

Application Number

212179

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 202042

Drug Name

EFAVIRENZ

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

202042 / 1

Active Ingredient

EFAVIRENZ

Application Number

202042

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 202042

Drug Name

EFAVIRENZ

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

202042 / 2

Active Ingredient

EFAVIRENZ

Application Number

202042

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 202301

Drug Name

EFAVIRENZ

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

-

202301 / 1

Active Ingredient

EFAVIRENZ

Application Number

202301

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 205389

Drug Name

EFAVIRENZ

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

205389 / 1

Active Ingredient

EFAVIRENZ

Application Number

205389

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 205389

Drug Name

EFAVIRENZ

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

-

205389 / 2

Active Ingredient

EFAVIRENZ

Application Number

205389

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 205389

Drug Name

EFAVIRENZ

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

-

205389 / 3

Active Ingredient

EFAVIRENZ

Application Number

205389

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 200406

Drug Name

LAMIVUDINE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

-

200406 / 1

Active Ingredient

LAMIVUDINE

Application Number

200406

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 200406

Drug Name

LAMIVUDINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

-

200406 / 2

Active Ingredient

LAMIVUDINE

Application Number

200406

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 206729

Drug Name

NEBIVOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

-

206729 / 1

Active Ingredient

NEBIVOLOL HYDROCHLORIDE

Application Number

206729

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 206729

Drug Name

NEBIVOLOL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

-

206729 / 2

Active Ingredient

NEBIVOLOL HYDROCHLORIDE

Application Number

206729

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 206729

Drug Name

NEBIVOLOL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

-

206729 / 3

Active Ingredient

NEBIVOLOL HYDROCHLORIDE

Application Number

206729

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 206729

Drug Name

NEBIVOLOL HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

-

206729 / 4

Active Ingredient

NEBIVOLOL HYDROCHLORIDE

Application Number

206729

Product Number

4

Dosage Form

-

Strength

20MG

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

BIMATOPROST

Application Number

204638

Product Number

1

Active Ingredient

BIMATOPROST

Dosage Form

-

Strength

0.01%

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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