Sagent Pharmaceuticals Discontinued
FDA Approved Drugs

Sagent Pharmaceuticals 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 9
  • Latest Approval Date Jul 16, 2025
  • Data Source FDA
  • First Approval Date Feb 08, 2006
All
52
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Unclassified
2
View
Discontinued
9
View
RX
41
View
Company Overview

Company

Sagent Pharmaceuticals Discontinued

Country

U.S.A

Website

Visit Website

Email

jsinger@sagentpharma.com

Social Profiles

Company Snapshot

Sagent Pharmaceuticals Discontinued

1901 N. Roselle Rd.Schaumburg, IL 60195

U.S.A

www.sagentpharma.com/ jsinger@sagentpharma.com View on Map
FDA Approved Drug Records ( 9 records )
2006
08 Feb
Discontinued Application: 77102

Drug Name

CALCITRIOL

Product Number

1

Dosage Form

-

Strength

0.001MG/ML

Approval Date

2006-02-08

77102 / 1

Active Ingredient

CALCITRIOL

Application Number

77102

Product Number

1

Dosage Form

-

Strength

0.001MG/ML

Approval Date

2006-02-08

Regulatory Status

Discontinued

2025
16 Jul
Discontinued Application: 219935

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

20MG/5ML (4MG/ML)

Approval Date

2025-07-16

219935 / 1

Active Ingredient

FAMOTIDINE

Application Number

219935

Product Number

1

Dosage Form

-

Strength

20MG/5ML (4MG/ML)

Approval Date

2025-07-16

Regulatory Status

Discontinued

2025
16 Jul
Discontinued Application: 219935

Drug Name

FAMOTIDINE

Product Number

2

Dosage Form

-

Strength

40MG/10ML (4MG/ML)

Approval Date

2025-07-16

219935 / 2

Active Ingredient

FAMOTIDINE

Application Number

219935

Product Number

2

Dosage Form

-

Strength

40MG/10ML (4MG/ML)

Approval Date

2025-07-16

Regulatory Status

Discontinued

2025
16 Jul
Discontinued Application: 219935

Drug Name

FAMOTIDINE

Product Number

3

Dosage Form

-

Strength

200MG/50ML (4MG/ML)

Approval Date

2025-07-16

219935 / 3

Active Ingredient

FAMOTIDINE

Application Number

219935

Product Number

3

Dosage Form

-

Strength

200MG/50ML (4MG/ML)

Approval Date

2025-07-16

Regulatory Status

Discontinued

2013
07 May
Discontinued Application: 91597

Drug Name

GEMCITABINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/VIAL

Approval Date

2013-05-07

91597 / 1

Active Ingredient

GEMCITABINE HYDROCHLORIDE

Application Number

91597

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/VIAL

Approval Date

2013-05-07

Regulatory Status

Discontinued

2013
07 May
Discontinued Application: 91597

Drug Name

GEMCITABINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2013-05-07

91597 / 2

Active Ingredient

GEMCITABINE HYDROCHLORIDE

Application Number

91597

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2013-05-07

Regulatory Status

Discontinued

2007
26 Mar
Discontinued Application: 78180

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2007-03-26

78180 / 1

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

78180

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2007-03-26

Regulatory Status

Discontinued

2012
30 Mar
Discontinued Application: 91246

Drug Name

OXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2012-03-30

91246 / 1

Active Ingredient

OXACILLIN SODIUM

Application Number

91246

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2012-03-30

Regulatory Status

Discontinued

2012
30 Mar
Discontinued Application: 91246

Drug Name

OXACILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2012-03-30

91246 / 2

Active Ingredient

OXACILLIN SODIUM

Application Number

91246

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2012-03-30

Regulatory Status

Discontinued

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Drug Status Breakdown
9 total
  • 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

CALCITRIOL

Application Number

77102

Product Number

1

Active Ingredient

CALCITRIOL

Dosage Form

-

Strength

0.001MG/ML

FDA Approved Drug Data

Approved drug product information

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