Marksans Pharma OTC
FDA Approved Drugs

Marksans Pharma OTC

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.

OTC
  • Total Records 19
  • Latest Approval Date Nov 17, 2025
  • Data Source FDA
  • First Approval Date Jun 26, 2009
All
38
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OTC
19
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RX
19
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Company Overview

Company

Marksans Pharma OTC

Country

India

Website

Visit Website

Email

info@marksanspharma.com

Social Profiles

Company Snapshot

Marksans Pharma OTC

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 )
2021
25 Aug
OTC Application: 215486

Drug Name

ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG

Approval Date

2021-08-25

215486 / 1

Active Ingredient

ACETAMINOPHEN

Application Number

215486

Product Number

1

Dosage Form

-

Strength

650MG

Approval Date

2021-08-25

Regulatory Status

OTC

2023
10 Jul
OTC Application: 216994

Drug Name

ACETAMINOPHEN AND IBUPROFEN

Product Number

1

Dosage Form

-

Strength

250MG;125MG

Approval Date

2023-07-10

216994 / 1

Active Ingredient

ACETAMINOPHEN; IBUPROFEN

Application Number

216994

Product Number

1

Dosage Form

-

Strength

250MG;125MG

Approval Date

2023-07-10

Regulatory Status

OTC

2010
15 Jun
OTC Application: 78933

Drug Name

CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2010-06-15

78933 / 1

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

78933

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2010-06-15

Regulatory Status

OTC

2010
15 Jun
OTC Application: 78933

Drug Name

CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2010-06-15

78933 / 2

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

78933

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2010-06-15

Regulatory Status

OTC

2010
15 Jun
OTC Application: 78933

Drug Name

CETIRIZINE HYDROCHLORIDE HIVES

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

2010-06-15

78933 / 3

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

78933

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

2010-06-15

Regulatory Status

OTC

2010
15 Jun
OTC Application: 78933

Drug Name

CETIRIZINE HYDROCHLORIDE HIVES

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2010-06-15

78933 / 4

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

78933

Product Number

4

Dosage Form

-

Strength

10MG

Approval Date

2010-06-15

Regulatory Status

OTC

2023
29 Sep
OTC Application: 217264

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2023-09-29

217264 / 1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

217264

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2023-09-29

Regulatory Status

OTC

2023
08 Mar
OTC Application: 217543

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2023-03-08

217543 / 1

Active Ingredient

FAMOTIDINE

Application Number

217543

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2023-03-08

Regulatory Status

OTC

2023
08 Mar
OTC Application: 217543

Drug Name

FAMOTIDINE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2023-03-08

217543 / 2

Active Ingredient

FAMOTIDINE

Application Number

217543

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2023-03-08

Regulatory Status

OTC

2023
21 Aug
OTC Application: 217780

Drug Name

GUAIFENESIN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2023-08-21

217780 / 1

Active Ingredient

GUAIFENESIN

Application Number

217780

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2023-08-21

Regulatory Status

OTC

2023
21 Aug
OTC Application: 217780

Drug Name

GUAIFENESIN

Product Number

2

Dosage Form

-

Strength

1.2GM

Approval Date

2023-08-21

217780 / 2

Active Ingredient

GUAIFENESIN

Application Number

217780

Product Number

2

Dosage Form

-

Strength

1.2GM

Approval Date

2023-08-21

Regulatory Status

OTC

2009
26 Jun
OTC Application: 79205

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

EQ 200MG FREE ACID AND POTASSIUM SALT

Approval Date

2009-06-26

79205 / 1

Active Ingredient

IBUPROFEN

Application Number

79205

Product Number

1

Dosage Form

-

Strength

EQ 200MG FREE ACID AND POTASSIUM SALT

Approval Date

2009-06-26

Regulatory Status

OTC

2011
08 Feb
OTC Application: 91237

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2011-02-08

91237 / 1

Active Ingredient

IBUPROFEN

Application Number

91237

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2011-02-08

Regulatory Status

OTC

2011
01 Feb
OTC Application: 91239

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2011-02-01

91239 / 1

Active Ingredient

IBUPROFEN

Application Number

91239

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2011-02-01

Regulatory Status

OTC

2025
17 Nov
OTC Application: 220153

Drug Name

LOPERAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2025-11-17

220153 / 1

Active Ingredient

LOPERAMIDE HYDROCHLORIDE

Application Number

220153

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2025-11-17

Regulatory Status

OTC

2016
23 Sep
OTC Application: 206214

Drug Name

LORATADINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2016-09-23

206214 / 1

Active Ingredient

LORATADINE

Application Number

206214

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2016-09-23

Regulatory Status

OTC

2024
21 Nov
OTC Application: 219223

Drug Name

LORATADINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2024-11-21

219223 / 1

Active Ingredient

LORATADINE

Application Number

219223

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2024-11-21

Regulatory Status

OTC

2011
16 Mar
OTC Application: 90545

Drug Name

NAPROXEN SODIUM

Product Number

1

Dosage Form

-

Strength

220MG

Approval Date

2011-03-16

90545 / 1

Active Ingredient

NAPROXEN SODIUM

Application Number

90545

Product Number

1

Dosage Form

-

Strength

220MG

Approval Date

2011-03-16

Regulatory Status

OTC

2025
07 Aug
OTC Application: 218829

Drug Name

OMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2025-08-07

218829 / 1

Active Ingredient

OMEPRAZOLE MAGNESIUM

Application Number

218829

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2025-08-07

Regulatory Status

OTC

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Drug Status Breakdown
19 total
  • OTC
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

ACETAMINOPHEN

Application Number

215486

Product Number

1

Active Ingredient

ACETAMINOPHEN

Dosage Form

-

Strength

650MG

FDA Approved Drug Data

Approved drug product information

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