Purdue Pharmaceuticals L.P
FDA Approved Drugs

Purdue Pharmaceuticals L.P

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 11
  • Latest Approval Date Jul 23, 2014
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Purdue Pharmaceuticals L.P

Country

U.S.A

Website

Visit Website

Email

Social Profiles

Company Snapshot

Purdue Pharmaceuticals L.P

One Stamford Forum, 201 Tresser Boulevard, Stamford, Connecticut 06901-3431

U.S.A

www.purduepharma.com/ View on Map
FDA Approved Drug Records ( 11 records )
1999
05 Aug
Discontinued Application: 20997

Drug Name

CHIROCAINE

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-08-05

20997 / 1

Active Ingredient

LEVOBUPIVACAINE HYDROCHLORIDE

Application Number

20997

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-08-05

Regulatory Status

Discontinued

1999
05 Aug
Discontinued Application: 20997

Drug Name

CHIROCAINE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-08-05

20997 / 2

Active Ingredient

LEVOBUPIVACAINE HYDROCHLORIDE

Application Number

20997

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-08-05

Regulatory Status

Discontinued

1999
05 Aug
Discontinued Application: 20997

Drug Name

CHIROCAINE

Product Number

3

Dosage Form

-

Strength

EQ 7.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-08-05

20997 / 3

Active Ingredient

LEVOBUPIVACAINE HYDROCHLORIDE

Application Number

20997

Product Number

3

Dosage Form

-

Strength

EQ 7.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-08-05

Regulatory Status

Discontinued

2004
24 Sep
Discontinued Application: 21044

Drug Name

PALLADONE

Product Number

1

Dosage Form

-

Strength

12MG

Approval Date

2004-09-24

21044 / 1

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

21044

Product Number

1

Dosage Form

-

Strength

12MG

Approval Date

2004-09-24

Regulatory Status

Discontinued

2004
24 Sep
Discontinued Application: 21044

Drug Name

PALLADONE

Product Number

2

Dosage Form

-

Strength

16MG

Approval Date

2004-09-24

21044 / 2

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

21044

Product Number

2

Dosage Form

-

Strength

16MG

Approval Date

2004-09-24

Regulatory Status

Discontinued

2004
24 Sep
Discontinued Application: 21044

Drug Name

PALLADONE

Product Number

3

Dosage Form

-

Strength

24MG

Approval Date

2004-09-24

21044 / 3

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

21044

Product Number

3

Dosage Form

-

Strength

24MG

Approval Date

2004-09-24

Regulatory Status

Discontinued

2004
24 Sep
Discontinued Application: 21044

Drug Name

PALLADONE

Product Number

4

Dosage Form

-

Strength

32MG

Approval Date

2004-09-24

21044 / 4

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

21044

Product Number

4

Dosage Form

-

Strength

32MG

Approval Date

2004-09-24

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 13092

Drug Name

SULFABID

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

13092 / 2

Active Ingredient

SULFAPHENAZOLE

Application Number

13092

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2014
23 Jul
Discontinued Application: 205777

Drug Name

TARGINIQ

Product Number

1

Dosage Form

-

Strength

5MG;10MG

Approval Date

2014-07-23

205777 / 1

Active Ingredient

NALOXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE

Application Number

205777

Product Number

1

Dosage Form

-

Strength

5MG;10MG

Approval Date

2014-07-23

Regulatory Status

Discontinued

2014
23 Jul
Discontinued Application: 205777

Drug Name

TARGINIQ

Product Number

2

Dosage Form

-

Strength

10MG;20MG

Approval Date

2014-07-23

205777 / 2

Active Ingredient

NALOXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE

Application Number

205777

Product Number

2

Dosage Form

-

Strength

10MG;20MG

Approval Date

2014-07-23

Regulatory Status

Discontinued

2014
23 Jul
Discontinued Application: 205777

Drug Name

TARGINIQ

Product Number

3

Dosage Form

-

Strength

20MG;40MG

Approval Date

2014-07-23

205777 / 3

Active Ingredient

NALOXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE

Application Number

205777

Product Number

3

Dosage Form

-

Strength

20MG;40MG

Approval Date

2014-07-23

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    11 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
11 total
  • Discontinued
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

CHIROCAINE

Application Number

20997

Product Number

1

Active Ingredient

LEVOBUPIVACAINE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 2.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit