Lannett Company, Inc. Unclassified
FDA Approved Drugs

Lannett Company, Inc. 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
67
View
Unclassified
10
View
Discontinued
45
View
RX
12
View
Company Overview

Company

Lannett Company, Inc. Unclassified

Country

U.S.A

Website

Visit Website

Email

customerservice@lannett.com

Social Profiles

Company Snapshot

Lannett Company, Inc. Unclassified

Lannett Company, Inc.13200 Townsend Road Philadelphia, PA 19154

U.S.A

www.lannett.com/ customerservice@lannett.com View on Map
FDA Approved Drug Records ( 10 records )
-
Unclassified Application: 65242

Drug Name

CLINDAMYCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

-

65242 / 1

Active Ingredient

CLINDAMYCIN HYDROCHLORIDE

Application Number

65242

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 65242

Drug Name

CLINDAMYCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

-

65242 / 2

Active Ingredient

CLINDAMYCIN HYDROCHLORIDE

Application Number

65242

Product Number

2

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78214

Drug Name

DANAZOL

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

78214 / 1

Active Ingredient

DANAZOL

Application Number

78214

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78214

Drug Name

DANAZOL

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

-

78214 / 2

Active Ingredient

DANAZOL

Application Number

78214

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 89740

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

-

89740 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

89740

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 89741

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

-

89741 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

89741

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 89742

Drug Name

FLUPHENAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

-

89742 / 1

Active Ingredient

FLUPHENAZINE HYDROCHLORIDE

Application Number

89742

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78439

Drug Name

HYDROMORPHONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

78439 / 1

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

78439

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78439

Drug Name

HYDROMORPHONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

-

78439 / 2

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

78439

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 84088

Drug Name

VELTANE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

-

84088 / 1

Active Ingredient

BROMPHENIRAMINE MALEATE

Application Number

84088

Product Number

1

Dosage Form

-

Strength

4MG

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

CLINDAMYCIN HYDROCHLORIDE

Application Number

65242

Product Number

1

Active Ingredient

CLINDAMYCIN HYDROCHLORIDE

Dosage Form

-

Strength

EQ 75MG 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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