Bayer AG Unclassified
FDA Approved Drugs

Bayer AG 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 23
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
277
View
Unclassified
23
View
Discontinued
190
View
OTC
4
View
RX
60
View
Company Overview

Company

Bayer AG Unclassified

Country

Germany

Website

Visit Website

Email

pharmachemicals@bayer.com

Social Profiles

Company Snapshot

Bayer AG Unclassified

Mullerstr. 178, 13353 Berlin

Germany

pharma.bayer.com/ pharmachemicals@bayer.com View on Map
FDA Approved Drug Records ( 23 records )
-
Unclassified Application: 21297

Drug Name

CLARINEX

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

-

21297 / 1

Active Ingredient

DESLORATADINE

Application Number

21297

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21363

Drug Name

CLARINEX

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

-

21363 / 1

Active Ingredient

DESLORATADINE

Application Number

21363

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21563

Drug Name

CLARINEX

Product Number

1

Dosage Form

-

Strength

0.5MG/ML

Approval Date

-

21563 / 1

Active Ingredient

DESLORATADINE

Application Number

21563

Product Number

1

Dosage Form

-

Strength

0.5MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103132

Drug Name

INTRON A

Product Number

1

Dosage Form

-

Strength

10MIU/VIAL

Approval Date

-

103132 / 1

Active Ingredient

INTERFERON ALFA-2B

Application Number

103132

Product Number

1

Dosage Form

-

Strength

10MIU/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103132

Drug Name

INTRON A

Product Number

2

Dosage Form

-

Strength

18MIU/VIAL

Approval Date

-

103132 / 2

Active Ingredient

INTERFERON ALFA-2B

Application Number

103132

Product Number

2

Dosage Form

-

Strength

18MIU/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103132

Drug Name

INTRON A

Product Number

3

Dosage Form

-

Strength

25MIU/VIAL

Approval Date

-

103132 / 3

Active Ingredient

INTERFERON ALFA-2B

Application Number

103132

Product Number

3

Dosage Form

-

Strength

25MIU/VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 20375

Drug Name

MENOSTAR

Product Number

7

Dosage Form

-

Strength

0.014MG/24HR

Approval Date

-

20375 / 7

Active Ingredient

ESTRADIOL

Application Number

20375

Product Number

7

Dosage Form

-

Strength

0.014MG/24HR

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 18181

Drug Name

MYCELEX

Product Number

2

Dosage Form

-

Strength

1%

Approval Date

-

18181 / 2

Active Ingredient

CLOTRIMAZOLE

Application Number

18181

Product Number

2

Dosage Form

-

Strength

1%

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 22027

Drug Name

NOXAFIL

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

-

22027 / 1

Active Ingredient

POSACONAZOLE

Application Number

22027

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

PEGINTRON

Product Number

1

Dosage Form

-

Strength

50UG/0.5ML

Approval Date

-

103949 / 1

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

1

Dosage Form

-

Strength

50UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

PEGINTRON

Product Number

2

Dosage Form

-

Strength

80UG/0.5ML

Approval Date

-

103949 / 2

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

2

Dosage Form

-

Strength

80UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

PEGINTRON

Product Number

3

Dosage Form

-

Strength

120UG/0.5ML

Approval Date

-

103949 / 3

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

3

Dosage Form

-

Strength

120UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

PEGINTRON

Product Number

4

Dosage Form

-

Strength

150UG/0.5ML

Approval Date

-

103949 / 4

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

4

Dosage Form

-

Strength

150UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

PEGINTRON

Product Number

5

Dosage Form

-

Strength

50UG/0.5ML

Approval Date

-

103949 / 5

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

5

Dosage Form

-

Strength

50UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

PEGINTRON

Product Number

6

Dosage Form

-

Strength

80UG/0.5ML

Approval Date

-

103949 / 6

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

6

Dosage Form

-

Strength

80UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

PEGINTRON

Product Number

7

Dosage Form

-

Strength

150UG/0.5ML

Approval Date

-

103949 / 7

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

7

Dosage Form

-

Strength

150UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

PEGINTRON

Product Number

8

Dosage Form

-

Strength

120UG/0.5ML

Approval Date

-

103949 / 8

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

8

Dosage Form

-

Strength

120UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

SYLATRON

Product Number

9

Dosage Form

-

Strength

296 MCG LYOPHILIZED POWDER PER SINGLE-USE VIAL

Approval Date

-

103949 / 9

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

9

Dosage Form

-

Strength

296 MCG LYOPHILIZED POWDER PER SINGLE-USE VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

SYLATRON

Product Number

10

Dosage Form

-

Strength

444 MCG LYOPHILIZED POWDER PER SINGLE-USE VIAL

Approval Date

-

103949 / 10

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

10

Dosage Form

-

Strength

444 MCG LYOPHILIZED POWDER PER SINGLE-USE VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103949

Drug Name

SYLATRON

Product Number

11

Dosage Form

-

Strength

888 MCG LYOPHILIZED POWDER PER SINGLE-USE VIAL

Approval Date

-

103949 / 11

Active Ingredient

PEGINTERFERON ALFA-2B

Application Number

103949

Product Number

11

Dosage Form

-

Strength

888 MCG LYOPHILIZED POWDER PER SINGLE-USE VIAL

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 20304

Drug Name

TRASYLOL

Product Number

1

Dosage Form

-

Strength

10,000KIU/ML

Approval Date

-

20304 / 1

Active Ingredient

APROTININ

Application Number

20304

Product Number

1

Dosage Form

-

Strength

10,000KIU/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 21873

Drug Name

YAZ

Product Number

1

Dosage Form

-

Strength

3MG; 0.02MG

Approval Date

-

21873 / 1

Active Ingredient

DROSPIRENONE; ETHINYL ESTRADIOL

Application Number

21873

Product Number

1

Dosage Form

-

Strength

3MG; 0.02MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 22045

Drug Name

YAZ

Product Number

1

Dosage Form

-

Strength

3MG; 0.02MG

Approval Date

-

22045 / 1

Active Ingredient

DROSPIRENONE; ETHINYL ESTRADIOL

Application Number

22045

Product Number

1

Dosage Form

-

Strength

3MG; 0.02MG

Approval Date

-

Regulatory Status

Unclassified

Related Databases
  • FDA Inspections
    43 View
  • EDQM CEP
    34 View
  • KDMF
    0 View
  • Japan DMF
    4 View
  • Eudra GMP
    0 View
  • NDC Database
    40 View
  • FDA Approved Drugs Database
    277 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
23 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

CLARINEX

Application Number

21297

Product Number

1

Active Ingredient

DESLORATADINE

Dosage Form

-

Strength

5MG

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