Lannett Company, Inc. RX
FDA Approved Drugs

Lannett Company, Inc. RX

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.

RX
  • Total Records 12
  • Latest Approval Date Feb 19, 2006
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
67
View
Unclassified
10
View
Discontinued
45
View
RX
12
View
Company Overview

Company

Lannett Company, Inc. RX

Country

U.S.A

Website

Visit Website

Email

customerservice@lannett.com

Social Profiles

Company Snapshot

Lannett Company, Inc. RX

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 ( 12 records )
1999
26 Feb
RX Application: 40230

Drug Name

DICYCLOMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1999-02-26

40230 / 1

Active Ingredient

DICYCLOMINE HYDROCHLORIDE

Application Number

40230

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1999-02-26

Regulatory Status

RX

1982
01 Jan
RX Application: 84285

Drug Name

DICYCLOMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

84285 / 1

Active Ingredient

DICYCLOMINE HYDROCHLORIDE

Application Number

84285

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 85372

Drug Name

DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Product Number

1

Dosage Form

-

Strength

0.025MG;2.5MG

Approval Date

1982-01-01

85372 / 1

Active Ingredient

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Application Number

85372

Product Number

1

Dosage Form

-

Strength

0.025MG;2.5MG

Approval Date

1982-01-01

Regulatory Status

RX

2001
03 Apr
RX Application: 21259

Drug Name

METADATE CD

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-03

21259 / 1

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-03

Regulatory Status

RX

2003
19 Jun
RX Application: 21259

Drug Name

METADATE CD

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2003-06-19

21259 / 2

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2003-06-19

Regulatory Status

RX

2003
27 May
RX Application: 21259

Drug Name

METADATE CD

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2003-05-27

21259 / 3

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2003-05-27

Regulatory Status

RX

2006
19 Feb
RX Application: 21259

Drug Name

METADATE CD

Product Number

4

Dosage Form

-

Strength

40MG

Approval Date

2006-02-19

21259 / 4

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

4

Dosage Form

-

Strength

40MG

Approval Date

2006-02-19

Regulatory Status

RX

2006
19 Feb
RX Application: 21259

Drug Name

METADATE CD

Product Number

5

Dosage Form

-

Strength

50MG

Approval Date

2006-02-19

21259 / 5

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

5

Dosage Form

-

Strength

50MG

Approval Date

2006-02-19

Regulatory Status

RX

2006
19 Feb
RX Application: 21259

Drug Name

METADATE CD

Product Number

6

Dosage Form

-

Strength

60MG

Approval Date

2006-02-19

21259 / 6

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21259

Product Number

6

Dosage Form

-

Strength

60MG

Approval Date

2006-02-19

Regulatory Status

RX

1982
01 Jan
RX Application: 84903

Drug Name

PRIMIDONE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

84903 / 1

Active Ingredient

PRIMIDONE

Application Number

84903

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

RX

2001
24 May
RX Application: 84903

Drug Name

PRIMIDONE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2001-05-24

84903 / 2

Active Ingredient

PRIMIDONE

Application Number

84903

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2001-05-24

Regulatory Status

RX

1982
01 Jan
RX Application: 80966

Drug Name

PROBALAN

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

80966 / 1

Active Ingredient

PROBENECID

Application Number

80966

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

RX

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Drug Status Breakdown
12 total
  • RX
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

DICYCLOMINE HYDROCHLORIDE

Application Number

40230

Product Number

1

Active Ingredient

DICYCLOMINE HYDROCHLORIDE

Dosage Form

-

Strength

20MG

FDA Approved Drug Data

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