ALRA
FDA Approved Drugs

ALRA

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 28
Latest Approval Date Aug 11, 1988
Data Source FDA
First Approval Date Jan 01, 1982

Company Overview

Company

ALRA

Country

United Kingdom

Website

Social Profiles

Company Snapshot

ALRA

United Kingdom

View on Map

FDA Approved Drug Records ( 28 records )

1982

01 Jan

Discontinued Application: 83320

Drug Name

ACETAZOLAMIDE

Product Number

Dosage Form

Strength

250MG

Approval Date

1982-01-01

83320 / 1 View Details

Active Ingredient

ACETAZOLAMIDE

Application Number

83320

Product Number

Dosage Form

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80380

Drug Name

BAMATE

Product Number

Dosage Form

Strength

200MG

Approval Date

1982-01-01

80380 / 1 View Details

Active Ingredient

MEPROBAMATE

Application Number

80380

Product Number

Dosage Form

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80380

Drug Name

BAMATE

Product Number

Dosage Form

Strength

400MG

Approval Date

1982-01-01

80380 / 2 View Details

Active Ingredient

MEPROBAMATE

Application Number

80380

Product Number

Dosage Form

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

26 Jul

Discontinued Application: 71331

Drug Name

CHOLAC

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

1988-07-26

71331 / 1 View Details

Active Ingredient

LACTULOSE

Application Number

71331

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

1988-07-26

Regulatory Status

Discontinued

1983

17 Aug

Discontinued Application: 84553

Drug Name

COMPOUND 65

Product Number

Dosage Form

Strength

389MG;32.4MG;65MG

Approval Date

1983-08-17

84553 / 2 View Details

Active Ingredient

ASPIRIN; CAFFEINE; PROPOXYPHENE HYDROCHLORIDE

Application Number

84553

Product Number

Dosage Form

Strength

389MG;32.4MG;65MG

Approval Date

1983-08-17

Regulatory Status

Discontinued

1988

26 Jul

Discontinued Application: 71054

Drug Name

CONSTILAC

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

1988-07-26

71054 / 1 View Details

Active Ingredient

LACTULOSE

Application Number

71054

Product Number

Dosage Form

Strength

10GM/15ML

Approval Date

1988-07-26

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80715

Drug Name

DIMENHYDRINATE

Product Number

Dosage Form

Strength

12.5MG/4ML

Approval Date

1982-01-01

80715 / 1 View Details

Active Ingredient

DIMENHYDRINATE

Application Number

80715

Product Number

Dosage Form

Strength

12.5MG/4ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80519

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

80519 / 3 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80519

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80519

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

80519 / 4 View Details

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

80519

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

15 Jun

Discontinued Application: 62758

Drug Name

ERYZOLE

Product Number

Dosage Form

Strength

EQ 200MG BASE/5ML;EQ 600MG BASE/5ML

Approval Date

1988-06-15

62758 / 1 View Details

Active Ingredient

ERYTHROMYCIN ETHYLSUCCINATE; SULFISOXAZOLE ACETYL

Application Number

62758

Product Number

Dosage Form

Strength

EQ 200MG BASE/5ML;EQ 600MG BASE/5ML

Approval Date

1988-06-15

Regulatory Status

Discontinued

1988

26 Apr

Discontinued Application: 71787

Drug Name

GEN-XENE

Product Number

Dosage Form

Strength

3.75MG

Approval Date

1988-04-26

71787 / 1 View Details

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71787

Product Number

Dosage Form

Strength

3.75MG

Approval Date

1988-04-26

Regulatory Status

Discontinued

1988

26 Apr

Discontinued Application: 71788

Drug Name

GEN-XENE

Product Number

Dosage Form

Strength

7.5MG

Approval Date

1988-04-26

71788 / 1 View Details

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71788

Product Number

Dosage Form

Strength

7.5MG

Approval Date

1988-04-26

Regulatory Status

Discontinued

1988

26 Apr

Discontinued Application: 71789

Drug Name

GEN-XENE

Product Number

Dosage Form

Strength

15MG

Approval Date

1988-04-26

71789 / 1 View Details

Active Ingredient

CLORAZEPATE DIPOTASSIUM

Application Number

71789

Product Number

Dosage Form

Strength

15MG

Approval Date

1988-04-26

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83554

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

83554 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

83554

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86369

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

86369 / 1 View Details

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

86369

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

11 Aug

Discontinued Application: 71058

Drug Name

IBU-TAB

Product Number

Dosage Form

Strength

400MG

Approval Date

1988-08-11

71058 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

71058

Product Number

Dosage Form

Strength

400MG

Approval Date

1988-08-11

Regulatory Status

Discontinued

1988

11 Aug

Discontinued Application: 71059

Drug Name

IBU-TAB

Product Number

Dosage Form

Strength

600MG

Approval Date

1988-08-11

71059 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

71059

Product Number

Dosage Form

Strength

600MG

Approval Date

1988-08-11

Regulatory Status

Discontinued

1988

11 Aug

Discontinued Application: 71965

Drug Name

IBU-TAB

Product Number

Dosage Form

Strength

800MG

Approval Date

1988-08-11

71965 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

71965

Product Number

Dosage Form

Strength

800MG

Approval Date

1988-08-11

Regulatory Status

Discontinued

1988

11 Aug

Discontinued Application: 71057

Drug Name

IBU-TAB 200

Product Number

Dosage Form

Strength

200MG

Approval Date

1988-08-11

71057 / 1 View Details

Active Ingredient

IBUPROFEN

Application Number

71057

Product Number

Dosage Form

Strength

200MG

Approval Date

1988-08-11

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85009

Drug Name

LYGEN

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

85009 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85009

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85107

Drug Name

LYGEN

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

85107 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85107

Product Number

Dosage Form

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 85108

Drug Name

LYGEN

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

85108 / 1 View Details

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85108

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83827

Drug Name

PRAMINE

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

83827 / 1 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

83827

Product Number

Dosage Form

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83827

Drug Name

PRAMINE

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

83827 / 2 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

83827

Product Number

Dosage Form

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83827

Drug Name

PRAMINE

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

83827 / 3 View Details

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

83827

Product Number

Dosage Form

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 83184

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

Dosage Form

Strength

65MG

Approval Date

1982-01-01

83184 / 1 View Details

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

83184

Product Number

Dosage Form

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 80366

Drug Name

SOXAZOLE

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

80366 / 1 View Details

Active Ingredient

SULFISOXAZOLE

Application Number

80366

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 86141

Drug Name

TOLBUTAMIDE

Product Number

Dosage Form

Strength

500MG

Approval Date

1982-01-01

86141 / 1 View Details

Active Ingredient

TOLBUTAMIDE

Application Number

86141

Product Number

Dosage Form

Strength

500MG

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
28 View
Drug Prices in Switzerland
0 View

Drug Status Breakdown

28 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

ACETAZOLAMIDE

Application Number

83320

Product Number

Active Ingredient

ACETAZOLAMIDE

Dosage Form

Strength

250MG

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.