Baxter Healthcare Corporation Unclassified
FDA Approved Drugs

Baxter Healthcare Corporation Unclassified

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.

Unclassified
  • Total Records 9
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
497
View
Unclassified
9
View
Discontinued
212
View
RX
276
View
Company Overview

Company

Baxter Healthcare Corporation Unclassified

Country

U.S.A

Website

Visit Website

Email

onebaxter@baxter.com

Social Profiles

Company Snapshot

Baxter Healthcare Corporation Unclassified

One Baxter Parkway Deerfield, IL 60015-4625

U.S.A

www.baxter.com/ onebaxter@baxter.com View on Map
FDA Approved Drug Records ( 9 records )
-
Unclassified Application: 22359

Drug Name

ARGATROBAN

Product Number

1

Dosage Form

-

Strength

250MG/250ML

Approval Date

-

22359 / 1

Active Ingredient

ARGATROBAN

Application Number

22359

Product Number

1

Dosage Form

-

Strength

250MG/250ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 19386

Drug Name

BREVIBLOC

Product Number

2

Dosage Form

-

Strength

250MG/ML

Approval Date

-

19386 / 2

Active Ingredient

ESMOLOL HYDROCHLORIDE

Application Number

19386

Product Number

2

Dosage Form

-

Strength

250MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 18609

Drug Name

HEPARIN SODIUM 2,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

2,000 UNITS/1000ML

Approval Date

-

18609 / 4

Active Ingredient

HEPARIN SODIUM

Application Number

18609

Product Number

4

Dosage Form

-

Strength

2,000 UNITS/1000ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 76427

Drug Name

MILRINONE LACTATE

Product Number

2

Dosage Form

-

Strength

20MG/20ML

Approval Date

-

76427 / 2

Active Ingredient

MILRINONE LACTATE

Application Number

76427

Product Number

2

Dosage Form

-

Strength

20MG/20ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 208157

Drug Name

MYXREDLIN

Product Number

1

Dosage Form

-

Strength

100 UNITS/100ML (1 UNIT/ML)

Approval Date

-

208157 / 1

Active Ingredient

INSULIN HUMAN

Application Number

208157

Product Number

1

Dosage Form

-

Strength

100 UNITS/100ML (1 UNIT/ML)

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 74812

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

20MEQ

Approval Date

-

74812 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

74812

Product Number

1

Dosage Form

-

Strength

20MEQ

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 74719

Drug Name

PROPOFOL

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

-

74719 / 1

Active Ingredient

PROPOFOL

Application Number

74719

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 75040

Drug Name

PROPOFOL

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

-

75040 / 1

Active Ingredient

PROPOFOL

Application Number

75040

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218524

Drug Name

SODIUM BICARBONATE

Product Number

1

Dosage Form

-

Strength

150MEQ/1000ML (0.150MEQ/ML)

Approval Date

-

218524 / 1

Active Ingredient

SODIUM BICARBONATE

Application Number

218524

Product Number

1

Dosage Form

-

Strength

150MEQ/1000ML (0.150MEQ/ML)

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
9 total
  • Unclassified
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

ARGATROBAN

Application Number

22359

Product Number

1

Active Ingredient

ARGATROBAN

Dosage Form

-

Strength

250MG/250ML

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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