Elite Laboratories, Inc. Discontinued
FDA Approved Drugs

Elite Laboratories, Inc. 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 4
  • Latest Approval Date Jan 22, 2003
  • Data Source FDA
  • First Approval Date Jun 18, 1997
All
60
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Discontinued
4
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RX
56
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Company Overview

Company

Elite Laboratories, Inc. Discontinued

Country

U.S.A

Website

Visit Website

Email

 info@elitepharma.com

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Company Snapshot

Elite Laboratories, Inc. Discontinued

165 Ludlow Avenue Northvale, New Jersey 07647, USA

U.S.A

elitepharma.com/  info@elitepharma.com View on Map
FDA Approved Drug Records ( 4 records )
1997
18 Jun
Discontinued Application: 40227

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1997-06-18

40227 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

40227

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1997-06-18

Regulatory Status

Discontinued

1997
19 Jun
Discontinued Application: 40228

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

1997-06-19

40228 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

40228

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

1997-06-19

Regulatory Status

Discontinued

2003
22 Jan
Discontinued Application: 40448

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2003-01-22

40448 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

40448

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2003-01-22

Regulatory Status

Discontinued

2003
14 Jan
Discontinued Application: 40460

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2003-01-14

40460 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

40460

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2003-01-14

Regulatory Status

Discontinued

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Drug Status Breakdown
4 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

PHENTERMINE HYDROCHLORIDE

Application Number

40227

Product Number

1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Dosage Form

-

Strength

30MG

FDA Approved Drug Data

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