Harman Finochem
FDA Approved Drugs

Harman Finochem

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 12
  • Latest Approval Date Jul 05, 2024
  • Data Source FDA
  • First Approval Date Dec 03, 2021
Company Overview

Company

Harman Finochem

Country

India

Website

Visit Website

Email

info@harmanfinochem.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Harman Finochem

107-A,Vinay Bhavya Complex, 159-A, C.S.T. Road, Kalina, Santacruz (East), Mumbai - 400 098, Maharashtra

India

harmanfinochem.com/ info@harmanfinochem.com View on Map
FDA Approved Drug Records ( 12 records )
2022
07 Mar
RX Application: 214443

Drug Name

ALLOPURINOL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2022-03-07

214443 / 1

Active Ingredient

ALLOPURINOL

Application Number

214443

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2022-03-07

Regulatory Status

RX

2022
07 Mar
RX Application: 214443

Drug Name

ALLOPURINOL

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2022-03-07

214443 / 2

Active Ingredient

ALLOPURINOL

Application Number

214443

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2022-03-07

Regulatory Status

RX

2024
17 Jun
RX Application: 214443

Drug Name

ALLOPURINOL

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2024-06-17

214443 / 3

Active Ingredient

ALLOPURINOL

Application Number

214443

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2024-06-17

Regulatory Status

RX

2024
18 Jan
RX Application: 217617

Drug Name

BISOPROLOL FUMARATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2024-01-18

217617 / 1

Active Ingredient

BISOPROLOL FUMARATE

Application Number

217617

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2024-01-18

Regulatory Status

RX

2024
18 Jan
RX Application: 217617

Drug Name

BISOPROLOL FUMARATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2024-01-18

217617 / 2

Active Ingredient

BISOPROLOL FUMARATE

Application Number

217617

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2024-01-18

Regulatory Status

RX

2021
03 Dec
RX Application: 213320

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2021-12-03

213320 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

213320

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2021-12-03

Regulatory Status

RX

2021
03 Dec
RX Application: 213320

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2021-12-03

213320 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

213320

Product Number

2

Dosage Form

-

Strength

850MG

Approval Date

2021-12-03

Regulatory Status

RX

2021
03 Dec
RX Application: 213320

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2021-12-03

213320 / 3

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

213320

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2021-12-03

Regulatory Status

RX

2024
05 Jul
RX Application: 218673

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2024-07-05

218673 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

218673

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2024-07-05

Regulatory Status

RX

2024
05 Jul
RX Application: 218673

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2024-07-05

218673 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

218673

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2024-07-05

Regulatory Status

RX

2023
24 Oct
RX Application: 214806

Drug Name

THEOPHYLLINE

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

2023-10-24

214806 / 1

Active Ingredient

THEOPHYLLINE

Application Number

214806

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

2023-10-24

Regulatory Status

RX

2023
24 Oct
RX Application: 214806

Drug Name

THEOPHYLLINE

Product Number

2

Dosage Form

-

Strength

450MG

Approval Date

2023-10-24

214806 / 2

Active Ingredient

THEOPHYLLINE

Application Number

214806

Product Number

2

Dosage Form

-

Strength

450MG

Approval Date

2023-10-24

Regulatory Status

RX

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Drug Status Breakdown
12 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

ALLOPURINOL

Application Number

214443

Product Number

1

Active Ingredient

ALLOPURINOL

Dosage Form

-

Strength

100MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

Structured Database

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