BioDelivery Sciences Discontinued
FDA Approved Drugs

BioDelivery Sciences Discontinued

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.

Discontinued
  • Total Records 3
  • Latest Approval Date Jun 06, 2014
  • Data Source FDA
  • First Approval Date Jun 06, 2014
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Discontinued
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RX
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Company

BioDelivery Sciences Discontinued

Country

U.S.A

Email

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Company Snapshot

BioDelivery Sciences Discontinued

4131 ParkLake Avenue, Suite 225 Raleigh, NC 27612

U.S.A

bdsi.com/ View on Map
FDA Approved Drug Records ( 3 records )
2014
06 Jun
Discontinued Application: 205637

Drug Name

BUNAVAIL

Product Number

1

Dosage Form

-

Strength

EQ 2.1MG BASE;EQ 0.3MG BASE

Approval Date

2014-06-06

205637 / 1

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

Application Number

205637

Product Number

1

Dosage Form

-

Strength

EQ 2.1MG BASE;EQ 0.3MG BASE

Approval Date

2014-06-06

Regulatory Status

Discontinued

2014
06 Jun
Discontinued Application: 205637

Drug Name

BUNAVAIL

Product Number

2

Dosage Form

-

Strength

EQ 4.2MG BASE;EQ 0.7MG BASE

Approval Date

2014-06-06

205637 / 2

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

Application Number

205637

Product Number

2

Dosage Form

-

Strength

EQ 4.2MG BASE;EQ 0.7MG BASE

Approval Date

2014-06-06

Regulatory Status

Discontinued

2014
06 Jun
Discontinued Application: 205637

Drug Name

BUNAVAIL

Product Number

3

Dosage Form

-

Strength

EQ 6.3MG BASE;EQ 1MG BASE

Approval Date

2014-06-06

205637 / 3

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

Application Number

205637

Product Number

3

Dosage Form

-

Strength

EQ 6.3MG BASE;EQ 1MG BASE

Approval Date

2014-06-06

Regulatory Status

Discontinued

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Drug Status Breakdown
3 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

BUNAVAIL

Application Number

205637

Product Number

1

Active Ingredient

BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 2.1MG BASE;EQ 0.3MG BASE

FDA Approved Drug Data

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