Nostrum Laboratories, Inc.
FDA Approved Drugs

Nostrum Laboratories, 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.

Discontinued RX
  • Total Records 20
  • Latest Approval Date Aug 09, 2023
  • Data Source FDA
  • First Approval Date Jan 11, 1983
All
20
View
Discontinued
14
View
RX
6
View
Company Overview

Company

Nostrum Laboratories, Inc.

Country

U.S.A

Website

Visit Website

Email

info@nostrumlabs.com

Social Profiles

Company Snapshot

Nostrum Laboratories, Inc.

Nostrum Laboratories, Inc. 1800 N Topping Ave Kansas City, MO 64120.

U.S.A

www.nostrumlabs.com/Default.aspx info@nostrumlabs.com View on Map
FDA Approved Drug Records ( 20 records )
1993
28 May
Discontinued Application: 73685

Drug Name

ACILAC

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1993-05-28

73685 / 1

Active Ingredient

LACTULOSE

Application Number

73685

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1993-05-28

Regulatory Status

Discontinued

1995
21 Feb
Discontinued Application: 74127

Drug Name

ATENOLOL

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1995-02-21

74127 / 1

Active Ingredient

ATENOLOL

Application Number

74127

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1995-02-21

Regulatory Status

Discontinued

1995
21 Feb
Discontinued Application: 74127

Drug Name

ATENOLOL

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1995-02-21

74127 / 2

Active Ingredient

ATENOLOL

Application Number

74127

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1995-02-21

Regulatory Status

Discontinued

1998
14 May
Discontinued Application: 74404

Drug Name

ATENOLOL AND CHLORTHALIDONE

Product Number

1

Dosage Form

-

Strength

50MG;25MG

Approval Date

1998-05-14

74404 / 1

Active Ingredient

ATENOLOL; CHLORTHALIDONE

Application Number

74404

Product Number

1

Dosage Form

-

Strength

50MG;25MG

Approval Date

1998-05-14

Regulatory Status

Discontinued

1998
14 May
Discontinued Application: 74404

Drug Name

ATENOLOL AND CHLORTHALIDONE

Product Number

2

Dosage Form

-

Strength

100MG;25MG

Approval Date

1998-05-14

74404 / 2

Active Ingredient

ATENOLOL; CHLORTHALIDONE

Application Number

74404

Product Number

2

Dosage Form

-

Strength

100MG;25MG

Approval Date

1998-05-14

Regulatory Status

Discontinued

2004
09 Jun
Discontinued Application: 76138

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

76138 / 1

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76138

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

2004
09 Jun
Discontinued Application: 76138

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

76138 / 2

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76138

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

2004
09 Jun
Discontinued Application: 76138

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

76138 / 3

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76138

Product Number

3

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

Regulatory Status

Discontinued

1993
28 May
Discontinued Application: 73686

Drug Name

LAXILOSE

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1993-05-28

73686 / 1

Active Ingredient

LACTULOSE

Application Number

73686

Product Number

1

Dosage Form

-

Strength

10GM/15ML

Approval Date

1993-05-28

Regulatory Status

Discontinued

2006
26 Jul
RX Application: 76756

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2006-07-26

76756 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

76756

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2006-07-26

Regulatory Status

RX

2011
12 Dec
RX Application: 76756

Drug Name

METFORMIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2011-12-12

76756 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

76756

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2011-12-12

Regulatory Status

RX

1996
28 Oct
Discontinued Application: 74474

Drug Name

PINDOLOL

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1996-10-28

74474 / 1

Active Ingredient

PINDOLOL

Application Number

74474

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1996-10-28

Regulatory Status

Discontinued

1996
28 Oct
Discontinued Application: 74474

Drug Name

PINDOLOL

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1996-10-28

74474 / 2

Active Ingredient

PINDOLOL

Application Number

74474

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1996-10-28

Regulatory Status

Discontinued

1983
11 Jan
RX Application: 87400

Drug Name

THEOPHYLLINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

1983-01-11

87400 / 2

Active Ingredient

THEOPHYLLINE

Application Number

87400

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

1983-01-11

Regulatory Status

RX

1985
21 Feb
RX Application: 87400

Drug Name

THEOPHYLLINE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

1985-02-21

87400 / 3

Active Ingredient

THEOPHYLLINE

Application Number

87400

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

1985-02-21

Regulatory Status

RX

1985
21 Feb
RX Application: 87400

Drug Name

THEOPHYLLINE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

1985-02-21

87400 / 4

Active Ingredient

THEOPHYLLINE

Application Number

87400

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

1985-02-21

Regulatory Status

RX

2023
09 Aug
RX Application: 87400

Drug Name

THEOPHYLLINE

Product Number

5

Dosage Form

-

Strength

450MG

Approval Date

2023-08-09

87400 / 5

Active Ingredient

THEOPHYLLINE

Application Number

87400

Product Number

5

Dosage Form

-

Strength

450MG

Approval Date

2023-08-09

Regulatory Status

RX

2023
04 Apr
Discontinued Application: 200430

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2023-04-04

200430 / 1

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

200430

Product Number

1

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2023-04-04

Regulatory Status

Discontinued

2023
04 Apr
Discontinued Application: 200430

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2023-04-04

200430 / 2

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

200430

Product Number

2

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2023-04-04

Regulatory Status

Discontinued

2023
04 Apr
Discontinued Application: 200430

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2023-04-04

200430 / 3

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

200430

Product Number

3

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2023-04-04

Regulatory Status

Discontinued

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Drug Status Breakdown
20 total
  • Discontinued
  • RX
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

ACILAC

Application Number

73685

Product Number

1

Active Ingredient

LACTULOSE

Dosage Form

-

Strength

10GM/15ML

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

Structured Database

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