Merck & Co Unclassified
FDA Approved Drugs

Merck & Co Unclassified

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.

Unclassified
  • Total Records 7
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
134
View
Unclassified
7
View
Discontinued
125
View
RX
2
View
Company Overview

Company

Merck & Co Unclassified

Country

U.S.A

Email

Social Profiles

Company Snapshot

Merck & Co Unclassified

One Merck Drive, P.O. Box 100 Whitehouse Station, NJ 08889-0100

U.S.A

www.merck.com/ View on Map
FDA Approved Drug Records ( 7 records )
-
Unclassified Application: 101063

Drug Name

ELSPAR

Product Number

1

Dosage Form

-

Strength

10,000IU/VIAL

Approval Date

-

101063 / 1

Active Ingredient

ASPARAGINASE

Application Number

101063

Product Number

1

Dosage Form

-

Strength

10,000IU/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 20888

Drug Name

LOTRIMIN AF

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

-

20888 / 1

Active Ingredient

CLOTRIMAZOLE

Application Number

20888

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 20889

Drug Name

LOTRIMIN AF

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

-

20889 / 1

Active Ingredient

CLOTRIMAZOLE

Application Number

20889

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 20890

Drug Name

LOTRIMIN AF

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

-

20890 / 1

Active Ingredient

CLOTRIMAZOLE

Application Number

20890

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21647

Drug Name

VIOXX

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

-

21647 / 1

Active Ingredient

ROFECOXIB

Application Number

21647

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21647

Drug Name

VIOXX

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

-

21647 / 2

Active Ingredient

ROFECOXIB

Application Number

21647

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21647

Drug Name

VIOXX

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

-

21647 / 3

Active Ingredient

ROFECOXIB

Application Number

21647

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
7 total
  • Unclassified
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

ELSPAR

Application Number

101063

Product Number

1

Active Ingredient

ASPARAGINASE

Dosage Form

-

Strength

10,000IU/VIAL

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

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