Merck Group
FDA Approved Drugs

Merck Group

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 11
  • Latest Approval Date Jun 16, 2005
  • Data Source FDA
  • First Approval Date Jun 16, 2005
Company Overview

Company

Merck Group

Country

Germany

Website

Visit Website

Email

service@merckgroup.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Merck Group

Frankfurter Strasse 250, 64293 Darmstadt

Germany

www.merckgroup.com/de service@merckgroup.com View on Map
FDA Approved Drug Records ( 11 records )
2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

1

Dosage Form

-

Strength

0.025MG

Approval Date

2005-06-16

76752 / 1

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

1

Dosage Form

-

Strength

0.025MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

2

Dosage Form

-

Strength

0.05MG

Approval Date

2005-06-16

76752 / 2

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

2

Dosage Form

-

Strength

0.05MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

3

Dosage Form

-

Strength

0.075MG

Approval Date

2005-06-16

76752 / 3

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

3

Dosage Form

-

Strength

0.075MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

4

Dosage Form

-

Strength

0.088MG

Approval Date

2005-06-16

76752 / 4

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

4

Dosage Form

-

Strength

0.088MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

5

Dosage Form

-

Strength

0.1MG

Approval Date

2005-06-16

76752 / 5

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

5

Dosage Form

-

Strength

0.1MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

6

Dosage Form

-

Strength

0.112MG

Approval Date

2005-06-16

76752 / 6

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

6

Dosage Form

-

Strength

0.112MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

7

Dosage Form

-

Strength

0.125MG

Approval Date

2005-06-16

76752 / 7

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

7

Dosage Form

-

Strength

0.125MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

8

Dosage Form

-

Strength

0.15MG

Approval Date

2005-06-16

76752 / 8

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

8

Dosage Form

-

Strength

0.15MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

9

Dosage Form

-

Strength

0.175MG

Approval Date

2005-06-16

76752 / 9

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

9

Dosage Form

-

Strength

0.175MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

10

Dosage Form

-

Strength

0.2MG

Approval Date

2005-06-16

76752 / 10

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

10

Dosage Form

-

Strength

0.2MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

2005
16 Jun
Discontinued Application: 76752

Drug Name

LEVOTHYROXINE SODIUM

Product Number

11

Dosage Form

-

Strength

0.3MG

Approval Date

2005-06-16

76752 / 11

Active Ingredient

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

11

Dosage Form

-

Strength

0.3MG

Approval Date

2005-06-16

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    14 View
  • KDMF
    0 View
  • Japan DMF
    6 View
  • Eudra GMP
    0 View
  • NDC Database
    38 View
  • FDA Approved Drugs Database
    11 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
11 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

LEVOTHYROXINE SODIUM

Application Number

76752

Product Number

1

Active Ingredient

LEVOTHYROXINE SODIUM

Dosage Form

-

Strength

0.025MG

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.
Login to Submit