Guangzhou Novaken Pharmaceutical
FDA Approved Drugs

Guangzhou Novaken Pharmaceutical

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 4
  • Latest Approval Date Jan 28, 2021
  • Data Source FDA
  • First Approval Date Nov 18, 2020
Company Overview

Company

Guangzhou Novaken Pharmaceutical

Country

China

Email

Social Profiles

Company Snapshot

Guangzhou Novaken Pharmaceutical

Health Industry Incubation Base, 280 East Circle, University Town, Guangzhou 510006

China

en.novaken.cn/ View on Map
FDA Approved Drug Records ( 4 records )
2020
18 Nov
RX Application: 213859

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2020-11-18

213859 / 1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

213859

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2020-11-18

Regulatory Status

RX

2020
18 Nov
RX Application: 213859

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2020-11-18

213859 / 2

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

213859

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2020-11-18

Regulatory Status

RX

2021
28 Jan
RX Application: 214395

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

2021-01-28

214395 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

214395

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

2021-01-28

Regulatory Status

RX

2021
28 Jan
RX Application: 214395

Drug Name

POTASSIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

20MEQ

Approval Date

2021-01-28

214395 / 2

Active Ingredient

POTASSIUM CHLORIDE

Application Number

214395

Product Number

2

Dosage Form

-

Strength

20MEQ

Approval Date

2021-01-28

Regulatory Status

RX

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Drug Status Breakdown
4 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

ESOMEPRAZOLE MAGNESIUM

Application Number

213859

Product Number

1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Dosage Form

-

Strength

EQ 20MG BASE

FDA Approved Drug Data

Approved drug product information

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