Meda Pharmaceuticals Inc. Discontinued
FDA Approved Drugs

Meda Pharmaceuticals 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 7
  • Latest Approval Date Jun 10, 2005
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
9
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Unclassified
2
View
Discontinued
7
View
Company Overview

Company

Meda Pharmaceuticals Inc. Discontinued

Country

U.S.A

Website

Visit Website

Email

 info@meda.us

Social Profiles

Company Snapshot

Meda Pharmaceuticals Inc. Discontinued

Meda Pharmaceuticals265 Davidson Ave. Somerset, NJ 08873-4120(732) 564-2200

U.S.A

www.meda.us/  info@meda.us View on Map
FDA Approved Drug Records ( 7 records )
1982
01 Jan
Discontinued Application: 85380

Drug Name

BUTISOL SODIUM

Product Number

1

Dosage Form

-

Strength

30MG/5ML

Approval Date

1982-01-01

85380 / 1

Active Ingredient

BUTABARBITAL SODIUM

Application Number

85380

Product Number

1

Dosage Form

-

Strength

30MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2005
10 Jun
Discontinued Application: 21793

Drug Name

REGLAN ODT

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2005-06-10

21793 / 1

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

21793

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2005-06-10

Regulatory Status

Discontinued

2005
10 Jun
Discontinued Application: 21793

Drug Name

REGLAN ODT

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2005-06-10

21793 / 2

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

21793

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2005-06-10

Regulatory Status

Discontinued

1990
18 Dec
Discontinued Application: 19919

Drug Name

ROWASA

Product Number

1

Dosage Form

-

Strength

500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1990-12-18

19919 / 1

Active Ingredient

MESALAMINE

Application Number

19919

Product Number

1

Dosage Form

-

Strength

500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1990-12-18

Regulatory Status

Discontinued

1983
11 Jul
Discontinued Application: 12365

Drug Name

SOMA COMPOUND

Product Number

5

Dosage Form

-

Strength

325MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-07-11

12365 / 5

Active Ingredient

ASPIRIN; CARISOPRODOL

Application Number

12365

Product Number

5

Dosage Form

-

Strength

325MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-07-11

Regulatory Status

Discontinued

1983
11 Jul
Discontinued Application: 12366

Drug Name

SOMA COMPOUND W/ CODEINE

Product Number

2

Dosage Form

-

Strength

325MG;200MG;16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-07-11

12366 / 2

Active Ingredient

ASPIRIN; CARISOPRODOL; CODEINE PHOSPHATE

Application Number

12366

Product Number

2

Dosage Form

-

Strength

325MG;200MG;16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-07-11

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18307

Drug Name

THYRO-BLOCK

Product Number

1

Dosage Form

-

Strength

130MG

Approval Date

1982-01-01

18307 / 1

Active Ingredient

POTASSIUM IODIDE

Application Number

18307

Product Number

1

Dosage Form

-

Strength

130MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
7 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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Drug Name

BUTISOL SODIUM

Application Number

85380

Product Number

1

Active Ingredient

BUTABARBITAL SODIUM

Dosage Form

-

Strength

30MG/5ML

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