Nexgen Pharma, Inc.
FDA Approved Drugs

Nexgen Pharma, 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 13
  • Latest Approval Date Sep 27, 2006
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Nexgen Pharma, Inc.

Country

U.S.A

Email

Social Profiles

Company Snapshot

Nexgen Pharma, Inc.

46 Corporate Park #100 Irvine, CA 92606

U.S.A

www.nexgenpharma.com/ View on Map
FDA Approved Drug Records ( 13 records )
1982
01 Jan
Discontinued Application: 86187

Drug Name

BROMPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

86187 / 1

Active Ingredient

BROMPHENIRAMINE MALEATE

Application Number

86187

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85985

Drug Name

DIMENHYDRINATE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

85985 / 1

Active Ingredient

DIMENHYDRINATE

Application Number

85985

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83634

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83634 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

83634

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84915

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

84915 / 1

Active Ingredient

FOLIC ACID

Application Number

84915

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83140

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

83140 / 1

Active Ingredient

HYDROCORTISONE

Application Number

83140

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84050

Drug Name

ISONIAZID

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84050 / 1

Active Ingredient

ISONIAZID

Application Number

84050

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86392

Drug Name

MECLIZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

86392 / 1

Active Ingredient

MECLIZINE HYDROCHLORIDE

Application Number

86392

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84220

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84220 / 1

Active Ingredient

MEPROBAMATE

Application Number

84220

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84589

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

84589 / 1

Active Ingredient

MEPROBAMATE

Application Number

84589

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86020

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

86020 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

86020

Product Number

1

Dosage Form

-

Strength

35MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2006
27 Sep
Discontinued Application: 77706

Drug Name

POLYETHYLENE GLYCOL 3350

Product Number

1

Dosage Form

-

Strength

17GM/SCOOPFUL

Approval Date

2006-09-27

77706 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350

Application Number

77706

Product Number

1

Dosage Form

-

Strength

17GM/SCOOPFUL

Approval Date

2006-09-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83185

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

83185 / 1

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

83185

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84238

Drug Name

SODIUM PENTOBARBITAL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84238 / 1

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

84238

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    13 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
13 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

BROMPHENIRAMINE MALEATE

Application Number

86187

Product Number

1

Active Ingredient

BROMPHENIRAMINE MALEATE

Dosage Form

-

Strength

4MG

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.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.