Sigmapharm Laboratories, LLC Discontinued
FDA Approved Drugs

Sigmapharm Laboratories, LLC 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 7
  • Latest Approval Date May 07, 2018
  • Data Source FDA
  • First Approval Date Jul 14, 2010
All
34
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Unclassified
2
View
Discontinued
7
View
RX
25
View
Company Overview

Company

Sigmapharm Laboratories, LLC Discontinued

Country

U.S.A

Website

Visit Website

Email

akotrotsios@sigmapharm.com

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Company Snapshot

Sigmapharm Laboratories, LLC Discontinued

Sigmapharm Laboratories, LLC 3375 Progress Drive Bensalem

U.S.A

www.sigmapharm.com/ akotrotsios@sigmapharm.com View on Map
FDA Approved Drug Records ( 7 records )
2010
14 Jul
Discontinued Application: 91004

Drug Name

ERGOCALCIFEROL

Product Number

1

Dosage Form

-

Strength

50,000 IU

Approval Date

2010-07-14

91004 / 1

Active Ingredient

ERGOCALCIFEROL

Application Number

91004

Product Number

1

Dosage Form

-

Strength

50,000 IU

Approval Date

2010-07-14

Regulatory Status

Discontinued

2018
07 May
Discontinued Application: 207745

Drug Name

NITROGLYCERIN

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

2018-05-07

207745 / 1

Active Ingredient

NITROGLYCERIN

Application Number

207745

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

2018-05-07

Regulatory Status

Discontinued

2018
07 May
Discontinued Application: 207745

Drug Name

NITROGLYCERIN

Product Number

2

Dosage Form

-

Strength

0.4MG

Approval Date

2018-05-07

207745 / 2

Active Ingredient

NITROGLYCERIN

Application Number

207745

Product Number

2

Dosage Form

-

Strength

0.4MG

Approval Date

2018-05-07

Regulatory Status

Discontinued

2018
07 May
Discontinued Application: 207745

Drug Name

NITROGLYCERIN

Product Number

3

Dosage Form

-

Strength

0.6MG

Approval Date

2018-05-07

207745 / 3

Active Ingredient

NITROGLYCERIN

Application Number

207745

Product Number

3

Dosage Form

-

Strength

0.6MG

Approval Date

2018-05-07

Regulatory Status

Discontinued

2016
19 Aug
Discontinued Application: 207528

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

8MEQ

Approval Date

2016-08-19

207528 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

207528

Product Number

1

Dosage Form

-

Strength

8MEQ

Approval Date

2016-08-19

Regulatory Status

Discontinued

2016
19 Aug
Discontinued Application: 207528

Drug Name

POTASSIUM CHLORIDE

Product Number

2

Dosage Form

-

Strength

10MEQ

Approval Date

2016-08-19

207528 / 2

Active Ingredient

POTASSIUM CHLORIDE

Application Number

207528

Product Number

2

Dosage Form

-

Strength

10MEQ

Approval Date

2016-08-19

Regulatory Status

Discontinued

2013
22 Mar
Discontinued Application: 202819

Drug Name

SODIUM PHENYLBUTYRATE

Product Number

1

Dosage Form

-

Strength

3GM/TEASPOONFUL

Approval Date

2013-03-22

202819 / 1

Active Ingredient

SODIUM PHENYLBUTYRATE

Application Number

202819

Product Number

1

Dosage Form

-

Strength

3GM/TEASPOONFUL

Approval Date

2013-03-22

Regulatory Status

Discontinued

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Drug Status Breakdown
7 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

ERGOCALCIFEROL

Application Number

91004

Product Number

1

Active Ingredient

ERGOCALCIFEROL

Dosage Form

-

Strength

50,000 IU

FDA Approved Drug Data

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