Hospira, Inc. Unclassified
FDA Approved Drugs

Hospira, Inc. 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 14
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
863
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Unclassified
14
View
Discontinued
561
View
RX
288
View
Company Overview

Company

Hospira, Inc. Unclassified

Country

U.S.A

Website

Visit Website

Email

supportservices@hospira.com

Social Profiles

LinkedIn
Company Snapshot

Hospira, Inc. Unclassified

275 North Field Drive, Lake Forest, Illinois

U.S.A

www.pfizerhospitalus.com/ supportservices@hospira.com View on Map
FDA Approved Drug Records ( 14 records )
-
Unclassified Application: 22046

Drug Name

BUPIVACAINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

-

22046 / 2

Active Ingredient

BUPIVACAINE HYDROCHLORIDE

Application Number

22046

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 203797

Drug Name

DAPTOMYCIN

Product Number

1

Dosage Form

-

Strength

350MG/VIAL

Approval Date

-

203797 / 1

Active Ingredient

DAPTOMYCIN

Application Number

203797

Product Number

1

Dosage Form

-

Strength

350MG/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 208908

Drug Name

EPINEPHRINE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML (EQ 1MG BASE/ML)

Approval Date

-

208908 / 1

Active Ingredient

EPINEPHRINE

Application Number

208908

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/ML (EQ 1MG BASE/ML)

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761080

Drug Name

NIVESTYM

Product Number

1

Dosage Form

-

Strength

300MCG/ML

Approval Date

-

761080 / 1

Active Ingredient

FILGRASTIM-AAFI

Application Number

761080

Product Number

1

Dosage Form

-

Strength

300MCG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761080

Drug Name

NIVESTYM

Product Number

2

Dosage Form

-

Strength

480MCG/1.6ML

Approval Date

-

761080 / 2

Active Ingredient

FILGRASTIM-AAFI

Application Number

761080

Product Number

2

Dosage Form

-

Strength

480MCG/1.6ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761080

Drug Name

NIVESTYM

Product Number

3

Dosage Form

-

Strength

300MCG/0.5ML

Approval Date

-

761080 / 3

Active Ingredient

FILGRASTIM-AAFI

Application Number

761080

Product Number

3

Dosage Form

-

Strength

300MCG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761080

Drug Name

NIVESTYM

Product Number

4

Dosage Form

-

Strength

480MCG/0.8ML

Approval Date

-

761080 / 4

Active Ingredient

FILGRASTIM-AAFI

Application Number

761080

Product Number

4

Dosage Form

-

Strength

480MCG/0.8ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761111

Drug Name

NYVEPRIA

Product Number

1

Dosage Form

-

Strength

6MG/0.6ML

Approval Date

-

761111 / 1

Active Ingredient

PEGFILGRASTIM-APGF

Application Number

761111

Product Number

1

Dosage Form

-

Strength

6MG/0.6ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125545

Drug Name

RETACRIT

Product Number

1

Dosage Form

-

Strength

2,000UNITS/ML

Approval Date

-

125545 / 1

Active Ingredient

EPOETIN ALFA-EPBX

Application Number

125545

Product Number

1

Dosage Form

-

Strength

2,000UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125545

Drug Name

RETACRIT

Product Number

2

Dosage Form

-

Strength

3,000UNITS/ML

Approval Date

-

125545 / 2

Active Ingredient

EPOETIN ALFA-EPBX

Application Number

125545

Product Number

2

Dosage Form

-

Strength

3,000UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125545

Drug Name

RETACRIT

Product Number

3

Dosage Form

-

Strength

4,000UNITS/ML

Approval Date

-

125545 / 3

Active Ingredient

EPOETIN ALFA-EPBX

Application Number

125545

Product Number

3

Dosage Form

-

Strength

4,000UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125545

Drug Name

RETACRIT

Product Number

4

Dosage Form

-

Strength

10,000UNITS/ML

Approval Date

-

125545 / 4

Active Ingredient

EPOETIN ALFA-EPBX

Application Number

125545

Product Number

4

Dosage Form

-

Strength

10,000UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125545

Drug Name

RETACRIT

Product Number

5

Dosage Form

-

Strength

40,000UNITS/ML

Approval Date

-

125545 / 5

Active Ingredient

EPOETIN ALFA-EPBX

Application Number

125545

Product Number

5

Dosage Form

-

Strength

40,000UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 90709

Drug Name

ZOLEDRONIC ACID

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE/5ML

Approval Date

-

90709 / 1

Active Ingredient

ZOLEDRONIC ACID

Application Number

90709

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE/5ML

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
14 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

BUPIVACAINE HYDROCHLORIDE

Application Number

22046

Product Number

2

Active Ingredient

BUPIVACAINE HYDROCHLORIDE

Dosage Form

-

Strength

0.5%

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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