UDL Laboratories Inc
FDA Approved Drugs

UDL 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
  • Total Records 7
  • Latest Approval Date Jun 13, 1983
  • Data Source FDA
  • First Approval Date Jan 18, 1983
Company Overview

Company

UDL Laboratories Inc

Country

U.S.A

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Company Snapshot

UDL Laboratories Inc

6700 Valjean Ave. Van Nuys, CA 91406

U.S.A

udlab.com/ cs@udlab.com View on Map
FDA Approved Drug Records ( 7 records )
1983
29 Mar
Discontinued Application: 88199

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1983-03-29

88199 / 1

Active Ingredient

FOLIC ACID

Application Number

88199

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1983-03-29

Regulatory Status

Discontinued

1983
13 Jun
Discontinued Application: 88256

Drug Name

MECLIZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1983-06-13

88256 / 1

Active Ingredient

MECLIZINE HYDROCHLORIDE

Application Number

88256

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

1983-06-13

Regulatory Status

Discontinued

1983
13 Jun
Discontinued Application: 88257

Drug Name

MECLIZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-06-13

88257 / 1

Active Ingredient

MECLIZINE HYDROCHLORIDE

Application Number

88257

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-06-13

Regulatory Status

Discontinued

1983
18 Jan
Discontinued Application: 87987

Drug Name

PREDNISOLONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1983-01-18

87987 / 1

Active Ingredient

PREDNISOLONE

Application Number

87987

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1983-01-18

Regulatory Status

Discontinued

1983
18 Jan
Discontinued Application: 87984

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1983-01-18

87984 / 1

Active Ingredient

PREDNISONE

Application Number

87984

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1983-01-18

Regulatory Status

Discontinued

1983
18 Jan
Discontinued Application: 87985

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1983-01-18

87985 / 1

Active Ingredient

PREDNISONE

Application Number

87985

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1983-01-18

Regulatory Status

Discontinued

1983
18 Jan
Discontinued Application: 87986

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1983-01-18

87986 / 1

Active Ingredient

PREDNISONE

Application Number

87986

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1983-01-18

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.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

FOLIC ACID

Application Number

88199

Product Number

1

Active Ingredient

FOLIC ACID

Dosage Form

-

Strength

1MG

FDA Approved Drug Data

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