Braeburn
FDA Approved Drugs

Braeburn

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 7
  • Latest Approval Date May 23, 2023
  • Data Source FDA
  • First Approval Date May 23, 2023
Company Overview

Company

Braeburn

Country

U.S.A

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Braeburn

450 Plymouth Rd, Suite 400 Plymouth Meeting, PA 19462

U.S.A

braeburnrx.com/ info@braeburnrx.com View on Map
FDA Approved Drug Records ( 7 records )
2023
23 May
RX Application: 210136

Drug Name

BRIXADI

Product Number

1

Dosage Form

-

Strength

8MG/0.16ML (50MG/ML)

Approval Date

2023-05-23

210136 / 1

Active Ingredient

BUPRENORPHINE

Application Number

210136

Product Number

1

Dosage Form

-

Strength

8MG/0.16ML (50MG/ML)

Approval Date

2023-05-23

Regulatory Status

RX

2023
23 May
RX Application: 210136

Drug Name

BRIXADI

Product Number

2

Dosage Form

-

Strength

16MG/0.32ML (50MG/ML)

Approval Date

2023-05-23

210136 / 2

Active Ingredient

BUPRENORPHINE

Application Number

210136

Product Number

2

Dosage Form

-

Strength

16MG/0.32ML (50MG/ML)

Approval Date

2023-05-23

Regulatory Status

RX

2023
23 May
RX Application: 210136

Drug Name

BRIXADI

Product Number

3

Dosage Form

-

Strength

24MG/0.48ML (50MG/ML)

Approval Date

2023-05-23

210136 / 3

Active Ingredient

BUPRENORPHINE

Application Number

210136

Product Number

3

Dosage Form

-

Strength

24MG/0.48ML (50MG/ML)

Approval Date

2023-05-23

Regulatory Status

RX

2023
23 May
RX Application: 210136

Drug Name

BRIXADI

Product Number

4

Dosage Form

-

Strength

32MG/0.64ML (50MG/ML)

Approval Date

2023-05-23

210136 / 4

Active Ingredient

BUPRENORPHINE

Application Number

210136

Product Number

4

Dosage Form

-

Strength

32MG/0.64ML (50MG/ML)

Approval Date

2023-05-23

Regulatory Status

RX

2023
23 May
RX Application: 210136

Drug Name

BRIXADI

Product Number

5

Dosage Form

-

Strength

64MG/0.18ML (356MG/ML)

Approval Date

2023-05-23

210136 / 5

Active Ingredient

BUPRENORPHINE

Application Number

210136

Product Number

5

Dosage Form

-

Strength

64MG/0.18ML (356MG/ML)

Approval Date

2023-05-23

Regulatory Status

RX

2023
23 May
RX Application: 210136

Drug Name

BRIXADI

Product Number

6

Dosage Form

-

Strength

96MG/0.27ML (356MG/ML)

Approval Date

2023-05-23

210136 / 6

Active Ingredient

BUPRENORPHINE

Application Number

210136

Product Number

6

Dosage Form

-

Strength

96MG/0.27ML (356MG/ML)

Approval Date

2023-05-23

Regulatory Status

RX

2023
23 May
RX Application: 210136

Drug Name

BRIXADI

Product Number

7

Dosage Form

-

Strength

128MG/0.36ML (356MG/ML)

Approval Date

2023-05-23

210136 / 7

Active Ingredient

BUPRENORPHINE

Application Number

210136

Product Number

7

Dosage Form

-

Strength

128MG/0.36ML (356MG/ML)

Approval Date

2023-05-23

Regulatory Status

RX

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Drug Status Breakdown
7 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

BRIXADI

Application Number

210136

Product Number

1

Active Ingredient

BUPRENORPHINE

Dosage Form

-

Strength

8MG/0.16ML (50MG/ML)

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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