CSPC-NBP Pharmaceutical
FDA Approved Drugs

CSPC-NBP 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 3
  • Latest Approval Date May 12, 2020
  • Data Source FDA
  • First Approval Date Jul 31, 2015
Company Overview

Company

CSPC-NBP Pharmaceutical

Country

China

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Company Snapshot

CSPC-NBP Pharmaceutical

88 Yangzi Road Economic Tech Dvpt Zone Shijiazhuang

China

www.nbp.com.cn/en/index.asp cspcnbp@mail.ecspc.com  View on Map
FDA Approved Drug Records ( 3 records )
2015
31 Jul
RX Application: 202765

Drug Name

BENZONATATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2015-07-31

202765 / 1

Active Ingredient

BENZONATATE

Application Number

202765

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2015-07-31

Regulatory Status

RX

2017
25 Aug
RX Application: 202765

Drug Name

BENZONATATE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2017-08-25

202765 / 2

Active Ingredient

BENZONATATE

Application Number

202765

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2017-08-25

Regulatory Status

RX

2020
12 May
RX Application: 211979

Drug Name

OMEGA-3-ACID ETHYL ESTERS

Product Number

1

Dosage Form

-

Strength

1GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS

Approval Date

2020-05-12

211979 / 1

Active Ingredient

OMEGA-3-ACID ETHYL ESTERS

Application Number

211979

Product Number

1

Dosage Form

-

Strength

1GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS

Approval Date

2020-05-12

Regulatory Status

RX

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Drug Status Breakdown
3 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

202765

Product Number

1

Active Ingredient

BENZONATATE

Dosage Form

-

Strength

200MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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