Morton Grove Pharmaceuticals, Inc.
FDA Approved Drugs

Morton Grove Pharmaceuticals, 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

Total Records 22
Latest Approval Date Sep 27, 1988
Data Source FDA
First Approval Date Nov 04, 1982

Company Overview

Company

Morton Grove Pharmaceuticals, Inc.

Country

U.S.A

Website

Visit Website

contactusa@wockhardt.com

Social Profiles

Company Snapshot

Morton Grove Pharmaceuticals, Inc.

Wockhardt USA, Wockhardt USA LLC, 20 Waterview Blvd., 3rd Floor Parsippany, NJ 07054

U.S.A

www.wockhardtusa.com/ contactusa@wockhardt.com View on Map

FDA Approved Drug Records ( 22 records )

1983

05 Dec

Discontinued Application: 88156

Drug Name

AMINOPHYLLINE

Product Number

Dosage Form

Strength

105MG/5ML

Approval Date

1983-12-05

88156 / 1 View Details

Active Ingredient

AMINOPHYLLINE

Application Number

88156

Product Number

Dosage Form

Strength

105MG/5ML

Approval Date

1983-12-05

Regulatory Status

Discontinued

1982

04 Nov

Discontinued Application: 87001

Drug Name

CYPROHEPTADINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

2MG/5ML

Approval Date

1982-11-04

87001 / 1 View Details

Active Ingredient

CYPROHEPTADINE HYDROCHLORIDE

Application Number

87001

Product Number

Dosage Form

Strength

2MG/5ML

Approval Date

1982-11-04

Regulatory Status

Discontinued

1985

01 Oct

Discontinued Application: 70118

Drug Name

DIPHEN

Product Number

Dosage Form

Strength

12.5MG/5ML

Approval Date

1985-10-01

70118 / 1 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

70118

Product Number

Dosage Form

Strength

12.5MG/5ML

Approval Date

1985-10-01

Regulatory Status

Discontinued

1988

27 Sep

Discontinued Application: 71842

Drug Name

GENERLAC

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

1988-09-27

71842 / 1 View Details

Active Ingredient

LACTULOSE

Application Number

71842

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

1988-09-27

Regulatory Status

Discontinued

1986

07 Mar

Discontinued Application: 70710

Drug Name

HALOPERIDOL

Product Number

Dosage Form

Strength

EQ 2MG BASE/ML

Approval Date

1986-03-07

70710 / 1 View Details

Active Ingredient

HALOPERIDOL LACTATE

Application Number

70710

Product Number

Dosage Form

Strength

EQ 2MG BASE/ML

Approval Date

1986-03-07

Regulatory Status

Discontinued

1988

20 Jun

Discontinued Application: 89661

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

Dosage Form

Strength

50MG/5ML

Approval Date

1988-06-20

89661 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

89661

Product Number

Dosage Form

Strength

50MG/5ML

Approval Date

1988-06-20

Regulatory Status

Discontinued

1988

22 Sep

Discontinued Application: 71841

Drug Name

LACTULOSE

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

1988-09-22

71841 / 1 View Details

Active Ingredient

LACTULOSE

Application Number

71841

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

1988-09-22

Regulatory Status

Discontinued

1987

13 Oct

Discontinued Application: 71656

Drug Name

METAPROTERENOL SULFATE

Product Number

Dosage Form

Strength

10MG/5ML

Approval Date

1987-10-13

71656 / 1 View Details

Active Ingredient

METAPROTERENOL SULFATE

Application Number

71656

Product Number

Dosage Form

Strength

10MG/5ML

Approval Date

1987-10-13

Regulatory Status

Discontinued

1987

06 Mar

Discontinued Application: 70949

Drug Name

METOCLOPRAMIDE HYDROCHLORIDE

Product Number

Dosage Form

Strength

EQ 5MG BASE/5ML

Approval Date

1987-03-06

70949 / 1 View Details

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

70949

Product Number

Dosage Form

Strength

EQ 5MG BASE/5ML

Approval Date

1987-03-06

Regulatory Status

Discontinued

1987

19 Nov

Discontinued Application: 62835

Drug Name

NYSTATIN

Product Number

Dosage Form

Strength

100,000 UNITS/ML

Approval Date

1987-11-19

62835 / 1 View Details

Active Ingredient

NYSTATIN

Application Number

62835

Product Number

Dosage Form

Strength

100,000 UNITS/ML

Approval Date

1987-11-19

Regulatory Status

Discontinued

1983

05 Dec

Discontinued Application: 88243

Drug Name

OXTRIPHYLLINE

Product Number

Dosage Form

Strength

100MG/5ML

Approval Date

1983-12-05

88243 / 1 View Details

Active Ingredient

OXTRIPHYLLINE

Application Number

88243

Product Number

Dosage Form

Strength

100MG/5ML

Approval Date

1983-12-05

Regulatory Status

Discontinued

1983

05 Dec

Discontinued Application: 88242

Drug Name

OXTRIPHYLLINE PEDIATRIC

Product Number

Dosage Form

Strength

50MG/5ML

Approval Date

1983-12-05

88242 / 1 View Details

Active Ingredient

OXTRIPHYLLINE

Application Number

88242

Product Number

Dosage Form

Strength

50MG/5ML

Approval Date

1983-12-05

Regulatory Status

Discontinued

1984

25 Oct

Discontinued Application: 88597

Drug Name

PROCHLORPERAZINE EDISYLATE

Product Number

Dosage Form

Strength

EQ 5MG BASE/5ML

Approval Date

1984-10-25

88597 / 1 View Details

Active Ingredient

PROCHLORPERAZINE EDISYLATE

Application Number

88597

Product Number

Dosage Form

Strength

EQ 5MG BASE/5ML

Approval Date

1984-10-25

Regulatory Status

Discontinued

1984

25 Oct

Discontinued Application: 88598

Drug Name

PROCHLORPERAZINE EDISYLATE

Product Number

Dosage Form

Strength

EQ 10MG BASE/ML

Approval Date

1984-10-25

88598 / 1 View Details

Active Ingredient

PROCHLORPERAZINE EDISYLATE

Application Number

88598

Product Number

Dosage Form

Strength

EQ 10MG BASE/ML

Approval Date

1984-10-25

Regulatory Status

Discontinued

1984

11 Sep

Discontinued Application: 88717

Drug Name

SODIUM POLYSTYRENE SULFONATE

Product Number

Dosage Form

Strength

15GM/60ML

Approval Date

1984-09-11

88717 / 1 View Details

Active Ingredient

SODIUM POLYSTYRENE SULFONATE

Application Number

88717

Product Number

Dosage Form

Strength

15GM/60ML

Approval Date

1984-09-11

Regulatory Status

Discontinued

1983

01 Sep

Discontinued Application: 88090

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.025%

Approval Date

1983-09-01

88090 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

88090

Product Number

Dosage Form

Strength

0.025%

Approval Date

1983-09-01

Regulatory Status

Discontinued

1983

01 Sep

Discontinued Application: 88091

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.1%

Approval Date

1983-09-01

88091 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

88091

Product Number

Dosage Form

Strength

0.1%

Approval Date

1983-09-01

Regulatory Status

Discontinued

1983

01 Sep

Discontinued Application: 88092

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.5%

Approval Date

1983-09-01

88092 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

88092

Product Number

Dosage Form

Strength

0.5%

Approval Date

1983-09-01

Regulatory Status

Discontinued

1983

01 Sep

Discontinued Application: 88094

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.025%

Approval Date

1983-09-01

88094 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

88094

Product Number

Dosage Form

Strength

0.025%

Approval Date

1983-09-01

Regulatory Status

Discontinued

1983

01 Sep

Discontinued Application: 88095

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.1%

Approval Date

1983-09-01

88095 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

88095

Product Number

Dosage Form

Strength

0.1%

Approval Date

1983-09-01

Regulatory Status

Discontinued

1983

01 Sep

Discontinued Application: 88096

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

Dosage Form

Strength

0.5%

Approval Date

1983-09-01

88096 / 1 View Details

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

88096

Product Number

Dosage Form

Strength

0.5%

Approval Date

1983-09-01

Regulatory Status

Discontinued

1985

11 Apr

Discontinued Application: 88285

Drug Name

TRIMEPRAZINE TARTRATE

Product Number

Dosage Form

Strength

EQ 2.5MG BASE/5ML

Approval Date

1985-04-11

88285 / 1 View Details

Active Ingredient

TRIMEPRAZINE TARTRATE

Application Number

88285

Product Number

Dosage Form

Strength

EQ 2.5MG BASE/5ML

Approval Date

1985-04-11

Regulatory Status

Discontinued

Related Databases

FDA Inspections
9 View
EDQM CEP
0 View
KDMF
0 View
Japan DMF
0 View
Eudra GMP
0 View
NDC Database
0 View
FDA Approved Drugs Database
22 View
Drug Prices in Switzerland
0 View

Drug Status Breakdown

22 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

AMINOPHYLLINE

Application Number

88156

Product Number

Active Ingredient

AMINOPHYLLINE

Dosage Form

Strength

105MG/5ML

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

Create a New Buying Request

Fields marked with * are mandatory.

Required Quantity *

Please enter quantity.

Measurement Unit *

Please select a unit.

Quality Standard *

Please select quality standard.

Request Type *

Please select request type.

Product Specifications *

Please provide product specifications.

Additional Details *

Please enter additional details.

Shipping Preference *

Please select shipping preference.

Expected Delivery Date

Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.