Bostal
FDA Approved Drugs

Bostal

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 9
  • Latest Approval Date Dec 06, 2021
  • Data Source FDA
  • First Approval Date Oct 21, 2011
Company Overview

Company

Bostal

Country

China

Website

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Email

BD@bostaldrug.com

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Company Snapshot

Bostal

Guangzhou, Guangdong

China

www.bostaldrug.com/en BD@bostaldrug.com View on Map
FDA Approved Drug Records ( 9 records )
2017
19 Dec
RX Application: 207803

Drug Name

FENOFIBRATE

Product Number

1

Dosage Form

-

Strength

54MG

Approval Date

2017-12-19

207803 / 1

Active Ingredient

FENOFIBRATE

Application Number

207803

Product Number

1

Dosage Form

-

Strength

54MG

Approval Date

2017-12-19

Regulatory Status

RX

2017
19 Dec
RX Application: 207803

Drug Name

FENOFIBRATE

Product Number

2

Dosage Form

-

Strength

160MG

Approval Date

2017-12-19

207803 / 2

Active Ingredient

FENOFIBRATE

Application Number

207803

Product Number

2

Dosage Form

-

Strength

160MG

Approval Date

2017-12-19

Regulatory Status

RX

2021
10 Feb
RX Application: 208476

Drug Name

FENOFIBRATE

Product Number

1

Dosage Form

-

Strength

48MG

Approval Date

2021-02-10

208476 / 1

Active Ingredient

FENOFIBRATE

Application Number

208476

Product Number

1

Dosage Form

-

Strength

48MG

Approval Date

2021-02-10

Regulatory Status

RX

2021
10 Feb
RX Application: 208476

Drug Name

FENOFIBRATE

Product Number

2

Dosage Form

-

Strength

145MG

Approval Date

2021-02-10

208476 / 2

Active Ingredient

FENOFIBRATE

Application Number

208476

Product Number

2

Dosage Form

-

Strength

145MG

Approval Date

2021-02-10

Regulatory Status

RX

2011
21 Oct
RX Application: 200958

Drug Name

METHOCARBAMOL

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2011-10-21

200958 / 1

Active Ingredient

METHOCARBAMOL

Application Number

200958

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2011-10-21

Regulatory Status

RX

2011
21 Oct
RX Application: 200958

Drug Name

METHOCARBAMOL

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2011-10-21

200958 / 2

Active Ingredient

METHOCARBAMOL

Application Number

200958

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2011-10-21

Regulatory Status

RX

2021
06 Dec
RX Application: 200958

Drug Name

METHOCARBAMOL

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2021-12-06

200958 / 3

Active Ingredient

METHOCARBAMOL

Application Number

200958

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

2021-12-06

Regulatory Status

RX

2019
20 May
RX Application: 210281

Drug Name

SOLIFENACIN SUCCINATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2019-05-20

210281 / 1

Active Ingredient

SOLIFENACIN SUCCINATE

Application Number

210281

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2019-05-20

Regulatory Status

RX

2019
20 May
RX Application: 210281

Drug Name

SOLIFENACIN SUCCINATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2019-05-20

210281 / 2

Active Ingredient

SOLIFENACIN SUCCINATE

Application Number

210281

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2019-05-20

Regulatory Status

RX

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Drug Status Breakdown
9 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

FENOFIBRATE

Application Number

207803

Product Number

1

Active Ingredient

FENOFIBRATE

Dosage Form

-

Strength

54MG

FDA Approved Drug Data

Approved drug product information

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