Marksans Pharma RX
FDA Approved Drugs

Marksans Pharma RX

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.

RX
  • Total Records 19
  • Latest Approval Date Mar 30, 2026
  • Data Source FDA
  • First Approval Date Aug 02, 2001
All
38
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OTC
19
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RX
19
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Company Overview

Company

Marksans Pharma RX

Country

India

Website

Visit Website

Email

info@marksanspharma.com

Social Profiles

Company Snapshot

Marksans Pharma RX

1st Floor, Bharat Tin Works Building, Opp. Vasant Oasis, Makwana Road, Near Keys Hotel, Marol, Andheri (East), Mumbai – 400059, Maharashtra

India

marksanspharma.com/ info@marksanspharma.com View on Map
FDA Approved Drug Records ( 19 records )
2026
30 Mar
RX Application: 220298

Drug Name

BENZONATATE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2026-03-30

220298 / 1

Active Ingredient

BENZONATATE

Application Number

220298

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2026-03-30

Regulatory Status

RX

2026
30 Mar
RX Application: 220298

Drug Name

BENZONATATE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2026-03-30

220298 / 2

Active Ingredient

BENZONATATE

Application Number

220298

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2026-03-30

Regulatory Status

RX

2002
29 Jan
RX Application: 75465

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-29

75465 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75465

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-29

Regulatory Status

RX

2002
29 Jan
RX Application: 75465

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-29

75465 / 2

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75465

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-29

Regulatory Status

RX

2001
02 Aug
RX Application: 75465

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2001-08-02

75465 / 3

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75465

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2001-08-02

Regulatory Status

RX

2011
21 Jul
RX Application: 90007

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2011-07-21

90007 / 1

Active Ingredient

GABAPENTIN

Application Number

90007

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2011-07-21

Regulatory Status

RX

2011
21 Jul
RX Application: 90007

Drug Name

GABAPENTIN

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2011-07-21

90007 / 2

Active Ingredient

GABAPENTIN

Application Number

90007

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2011-07-21

Regulatory Status

RX

2011
21 Jul
RX Application: 90007

Drug Name

GABAPENTIN

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2011-07-21

90007 / 3

Active Ingredient

GABAPENTIN

Application Number

90007

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2011-07-21

Regulatory Status

RX

2010
21 Dec
RX Application: 90796

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

2010-12-21

90796 / 1

Active Ingredient

IBUPROFEN

Application Number

90796

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

2010-12-21

Regulatory Status

RX

2010
21 Dec
RX Application: 90796

Drug Name

IBUPROFEN

Product Number

2

Dosage Form

-

Strength

600MG

Approval Date

2010-12-21

90796 / 2

Active Ingredient

IBUPROFEN

Application Number

90796

Product Number

2

Dosage Form

-

Strength

600MG

Approval Date

2010-12-21

Regulatory Status

RX

2010
21 Dec
RX Application: 90796

Drug Name

IBUPROFEN

Product Number

3

Dosage Form

-

Strength

800MG

Approval Date

2010-12-21

90796 / 3

Active Ingredient

IBUPROFEN

Application Number

90796

Product Number

3

Dosage Form

-

Strength

800MG

Approval Date

2010-12-21

Regulatory Status

RX

2016
29 Apr
RX Application: 90295

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2016-04-29

90295 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

90295

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2016-04-29

Regulatory Status

RX

2016
29 Apr
RX Application: 90295

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2016-04-29

90295 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

90295

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2016-04-29

Regulatory Status

RX

2012
12 Mar
RX Application: 90888

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2012-03-12

90888 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

90888

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2012-03-12

Regulatory Status

RX

2012
12 Mar
RX Application: 90888

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2012-03-12

90888 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

90888

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2012-03-12

Regulatory Status

RX

2012
12 Mar
RX Application: 90888

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2012-03-12

90888 / 3

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

90888

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2012-03-12

Regulatory Status

RX

2016
07 Oct
RX Application: 204948

Drug Name

PARICALCITOL

Product Number

1

Dosage Form

-

Strength

1MCG

Approval Date

2016-10-07

204948 / 1

Active Ingredient

PARICALCITOL

Application Number

204948

Product Number

1

Dosage Form

-

Strength

1MCG

Approval Date

2016-10-07

Regulatory Status

RX

2016
07 Oct
RX Application: 204948

Drug Name

PARICALCITOL

Product Number

2

Dosage Form

-

Strength

2MCG

Approval Date

2016-10-07

204948 / 2

Active Ingredient

PARICALCITOL

Application Number

204948

Product Number

2

Dosage Form

-

Strength

2MCG

Approval Date

2016-10-07

Regulatory Status

RX

2016
07 Oct
RX Application: 204948

Drug Name

PARICALCITOL

Product Number

3

Dosage Form

-

Strength

4MCG

Approval Date

2016-10-07

204948 / 3

Active Ingredient

PARICALCITOL

Application Number

204948

Product Number

3

Dosage Form

-

Strength

4MCG

Approval Date

2016-10-07

Regulatory Status

RX

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Drug Status Breakdown
19 total
  • RX
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

BENZONATATE

Application Number

220298

Product Number

1

Active Ingredient

BENZONATATE

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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