Caraco Pharmaceutical Laboratories, Ltd. Discontinued
FDA Approved Drugs

Caraco Pharmaceutical Laboratories, Ltd. 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 8
  • Latest Approval Date Dec 23, 2008
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
17
View
Unclassified
9
View
Discontinued
8
View
Company Overview

Company

Caraco Pharmaceutical Laboratories, Ltd. Discontinued

Country

U.S.A

Website

Visit Website

Email

Sales@sunpharmausa.com

Social Profiles

Company Snapshot

Caraco Pharmaceutical Laboratories, Ltd. Discontinued

1150 Elijah McCoy Drive, Detroit, MI 48202

U.S.A

www.caraco.com/ Sales@sunpharmausa.com View on Map
FDA Approved Drug Records ( 8 records )
2008
23 Dec
Discontinued Application: 90265

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

2008-12-23

90265 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

90265

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

2008-12-23

Regulatory Status

Discontinued

2008
23 Dec
Discontinued Application: 90265

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

2008-12-23

90265 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

90265

Product Number

2

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

2008-12-23

Regulatory Status

Discontinued

2008
23 Dec
Discontinued Application: 90265

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

3

Dosage Form

-

Strength

500MG;10MG

Approval Date

2008-12-23

90265 / 3

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

90265

Product Number

3

Dosage Form

-

Strength

500MG;10MG

Approval Date

2008-12-23

Regulatory Status

Discontinued

2008
23 Dec
Discontinued Application: 90380

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

2008-12-23

90380 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

90380

Product Number

1

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

2008-12-23

Regulatory Status

Discontinued

2008
23 Dec
Discontinued Application: 90380

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

650MG;10MG

Approval Date

2008-12-23

90380 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

90380

Product Number

2

Dosage Form

-

Strength

650MG;10MG

Approval Date

2008-12-23

Regulatory Status

Discontinued

2008
23 Dec
Discontinued Application: 90380

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

3

Dosage Form

-

Strength

660MG;10MG

Approval Date

2008-12-23

90380 / 3

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

90380

Product Number

3

Dosage Form

-

Strength

660MG;10MG

Approval Date

2008-12-23

Regulatory Status

Discontinued

2008
23 Dec
Discontinued Application: 90380

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

4

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

2008-12-23

90380 / 4

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

90380

Product Number

4

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

2008-12-23

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84999

Drug Name

WYGESIC

Product Number

1

Dosage Form

-

Strength

650MG;65MG

Approval Date

1982-01-01

84999 / 1

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE

Application Number

84999

Product Number

1

Dosage Form

-

Strength

650MG;65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
8 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

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Application Number

90265

Product Number

1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Dosage Form

-

Strength

500MG;5MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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