Impax Laboratories Unclassified
FDA Approved Drugs

Impax Laboratories Unclassified

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.

Unclassified
  • Total Records 10
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
283
View
Unclassified
10
View
Discontinued
160
View
RX
113
View
Company Overview

Company

Impax Laboratories Unclassified

Country

U.S.A

Website

Visit Website

Email

inquiries@impaxlabs.com

Social Profiles

Company Snapshot

Impax Laboratories Unclassified

30831 Huntwood Ave.Hayward, CA 94544

U.S.A

www.impaxlabs.com/ inquiries@impaxlabs.com View on Map
FDA Approved Drug Records ( 10 records )
-
Unclassified Application: 90669

Drug Name

DULOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

-

90669 / 1

Active Ingredient

DULOXETINE HYDROCHLORIDE

Application Number

90669

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 90669

Drug Name

DULOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

-

90669 / 2

Active Ingredient

DULOXETINE HYDROCHLORIDE

Application Number

90669

Product Number

2

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 90669

Drug Name

DULOXETINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 60MG BASE

Approval Date

-

90669 / 3

Active Ingredient

DULOXETINE HYDROCHLORIDE

Application Number

90669

Product Number

3

Dosage Form

-

Strength

EQ 60MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76318

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

-

76318 / 1

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

76318

Product Number

1

Dosage Form

-

Strength

80MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76446

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

-

76446 / 1

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

76446

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76446

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

-

76446 / 2

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

76446

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76446

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

-

76446 / 3

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

76446

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78057

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

-

78057 / 1

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

78057

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78057

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

75MG

Approval Date

-

78057 / 2

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

78057

Product Number

2

Dosage Form

-

Strength

75MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78057

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

-

78057 / 3

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

78057

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
10 total
  • Unclassified
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

DULOXETINE HYDROCHLORIDE

Application Number

90669

Product Number

1

Active Ingredient

DULOXETINE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 20MG BASE

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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