Medefil, Inc. Discontinued
FDA Approved Drugs

Medefil, 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 5
  • Latest Approval Date Jan 06, 2012
  • Data Source FDA
  • First Approval Date Jan 06, 2012
All
13
View
Discontinued
5
View
RX
8
View
Company Overview

Company

Medefil, Inc. Discontinued

Country

U.S.A

Website

Visit Website

Email

info@medefilinc.com

Social Profiles

Company Snapshot

Medefil, Inc. Discontinued

Corporate Headquarters Medefil, Inc. 250 Windy Point Drive Glendale Heights, IL 60139

U.S.A

www.medefilinc.com/ info@medefilinc.com View on Map
FDA Approved Drug Records ( 5 records )
2012
06 Jan
Discontinued Application: 202832

Drug Name

SODIUM CHLORIDE 0.9%

Product Number

1

Dosage Form

-

Strength

9MG/ML (9MG/ML)

Approval Date

2012-01-06

202832 / 1

Active Ingredient

SODIUM CHLORIDE

Application Number

202832

Product Number

1

Dosage Form

-

Strength

9MG/ML (9MG/ML)

Approval Date

2012-01-06

Regulatory Status

Discontinued

2012
06 Jan
Discontinued Application: 202832

Drug Name

SODIUM CHLORIDE 0.9%

Product Number

2

Dosage Form

-

Strength

18MG/2ML (9MG/ML)

Approval Date

2012-01-06

202832 / 2

Active Ingredient

SODIUM CHLORIDE

Application Number

202832

Product Number

2

Dosage Form

-

Strength

18MG/2ML (9MG/ML)

Approval Date

2012-01-06

Regulatory Status

Discontinued

2012
06 Jan
Discontinued Application: 202832

Drug Name

SODIUM CHLORIDE 0.9%

Product Number

3

Dosage Form

-

Strength

22.5MG/2.5ML (9MG/ML)

Approval Date

2012-01-06

202832 / 3

Active Ingredient

SODIUM CHLORIDE

Application Number

202832

Product Number

3

Dosage Form

-

Strength

22.5MG/2.5ML (9MG/ML)

Approval Date

2012-01-06

Regulatory Status

Discontinued

2012
06 Jan
Discontinued Application: 202832

Drug Name

SODIUM CHLORIDE 0.9%

Product Number

4

Dosage Form

-

Strength

27MG/3ML (9MG/ML)

Approval Date

2012-01-06

202832 / 4

Active Ingredient

SODIUM CHLORIDE

Application Number

202832

Product Number

4

Dosage Form

-

Strength

27MG/3ML (9MG/ML)

Approval Date

2012-01-06

Regulatory Status

Discontinued

2012
06 Jan
Discontinued Application: 202832

Drug Name

SODIUM CHLORIDE 0.9%

Product Number

5

Dosage Form

-

Strength

45MG/5ML (9MG/ML)

Approval Date

2012-01-06

202832 / 5

Active Ingredient

SODIUM CHLORIDE

Application Number

202832

Product Number

5

Dosage Form

-

Strength

45MG/5ML (9MG/ML)

Approval Date

2012-01-06

Regulatory Status

Discontinued

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Drug Status Breakdown
5 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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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

SODIUM CHLORIDE 0.9%

Application Number

202832

Product Number

1

Active Ingredient

SODIUM CHLORIDE

Dosage Form

-

Strength

9MG/ML (9MG/ML)

FDA Approved Drug Data

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