Medefil, Inc.
FDA Approved Drugs

Medefil, Inc.

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 Discontinued
  • Total Records 13
  • Latest Approval Date Nov 04, 2022
  • Data Source FDA
  • First Approval Date Jan 06, 2012
All
13
View
Discontinued
5
View
RX
8
View
Company Overview

Company

Medefil, Inc.

Country

U.S.A

Social Profiles

Company Snapshot

Medefil, Inc.

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 ( 13 records )
2022
04 Nov
RX Application: 214970

Drug Name

ATROPINE SULFATE

Product Number

1

Dosage Form

-

Strength

1MG/10ML (0.1MG/ML)

Approval Date

2022-11-04

214970 / 1

Active Ingredient

ATROPINE SULFATE

Application Number

214970

Product Number

1

Dosage Form

-

Strength

1MG/10ML (0.1MG/ML)

Approval Date

2022-11-04

Regulatory Status

RX

2019
01 May
RX Application: 211553

Drug Name

CALCIUM CHLORIDE 10%

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

2019-05-01

211553 / 1

Active Ingredient

CALCIUM CHLORIDE

Application Number

211553

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

2019-05-01

Regulatory Status

RX

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

2012
06 Jan
RX Application: 202832

Drug Name

SODIUM CHLORIDE 0.9%

Product Number

6

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

2012-01-06

202832 / 6

Active Ingredient

SODIUM CHLORIDE

Application Number

202832

Product Number

6

Dosage Form

-

Strength

90MG/10ML (9MG/ML)

Approval Date

2012-01-06

Regulatory Status

RX

2019
02 Dec
RX Application: 211188

Drug Name

STERILE WATER FOR INJECTION

Product Number

1

Dosage Form

-

Strength

100% (1ML)

Approval Date

2019-12-02

211188 / 1

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

211188

Product Number

1

Dosage Form

-

Strength

100% (1ML)

Approval Date

2019-12-02

Regulatory Status

RX

2019
02 Dec
RX Application: 211188

Drug Name

STERILE WATER FOR INJECTION

Product Number

2

Dosage Form

-

Strength

100% (2.5ML)

Approval Date

2019-12-02

211188 / 2

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

211188

Product Number

2

Dosage Form

-

Strength

100% (2.5ML)

Approval Date

2019-12-02

Regulatory Status

RX

2019
02 Dec
RX Application: 211188

Drug Name

STERILE WATER FOR INJECTION

Product Number

3

Dosage Form

-

Strength

100% (3ML)

Approval Date

2019-12-02

211188 / 3

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

211188

Product Number

3

Dosage Form

-

Strength

100% (3ML)

Approval Date

2019-12-02

Regulatory Status

RX

2019
02 Dec
RX Application: 211188

Drug Name

STERILE WATER FOR INJECTION

Product Number

4

Dosage Form

-

Strength

100% (5ML)

Approval Date

2019-12-02

211188 / 4

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

211188

Product Number

4

Dosage Form

-

Strength

100% (5ML)

Approval Date

2019-12-02

Regulatory Status

RX

2019
02 Dec
RX Application: 211188

Drug Name

STERILE WATER FOR INJECTION

Product Number

5

Dosage Form

-

Strength

100% (10ML)

Approval Date

2019-12-02

211188 / 5

Active Ingredient

STERILE WATER FOR INJECTION

Application Number

211188

Product Number

5

Dosage Form

-

Strength

100% (10ML)

Approval Date

2019-12-02

Regulatory Status

RX

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Drug Status Breakdown
13 total
  • RX
  • 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

ATROPINE SULFATE

Application Number

214970

Product Number

1

Active Ingredient

ATROPINE SULFATE

Dosage Form

-

Strength

1MG/10ML (0.1MG/ML)

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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