Annora Pharma Unclassified
FDA Approved Drugs

Annora Pharma 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 10
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
120
View
Unclassified
10
View
OTC
6
View
RX
104
View
Company Overview

Company

Annora Pharma Unclassified

Country

India

Website

Visit Website

Email

info@annorapharma.com

Social Profiles

Company Snapshot

Annora Pharma Unclassified

Sy. No. 261, Annaram Village, Gummadidal Mandal Sangareddy District. Telangana State – 502313

India

www.annorapharma.com/ info@annorapharma.com View on Map
FDA Approved Drug Records ( 10 records )
-
Unclassified Application: 214831

Drug Name

BRIVARACETAM

Product Number

2

Dosage Form

-

Strength

25mg

Approval Date

-

214831 / 2

Active Ingredient

BRIVARACETAM

Application Number

214831

Product Number

2

Dosage Form

-

Strength

25mg

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214831

Drug Name

BRIVARACETAM

Product Number

3

Dosage Form

-

Strength

50mg

Approval Date

-

214831 / 3

Active Ingredient

BRIVARACETAM

Application Number

214831

Product Number

3

Dosage Form

-

Strength

50mg

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214831

Drug Name

BRIVARACETAM

Product Number

4

Dosage Form

-

Strength

75mg

Approval Date

-

214831 / 4

Active Ingredient

BRIVARACETAM

Application Number

214831

Product Number

4

Dosage Form

-

Strength

75mg

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 214831

Drug Name

BRIVARACETAM

Product Number

5

Dosage Form

-

Strength

100mg

Approval Date

-

214831 / 5

Active Ingredient

BRIVARACETAM

Application Number

214831

Product Number

5

Dosage Form

-

Strength

100mg

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 212365

Drug Name

EMPAGLIFLOZIN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

-

212365 / 1

Active Ingredient

EMPAGLIFLOZIN

Application Number

212365

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 212365

Drug Name

EMPAGLIFLOZIN

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

-

212365 / 2

Active Ingredient

EMPAGLIFLOZIN

Application Number

212365

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 212364

Drug Name

EMPAGLIFLOZIN; LINAGLIPTIN

Product Number

1

Dosage Form

-

Strength

10MG; 5MG

Approval Date

-

212364 / 1

Active Ingredient

EMPAGLIFLOZIN;LINAGLIPTIN

Application Number

212364

Product Number

1

Dosage Form

-

Strength

10MG; 5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 212364

Drug Name

EMPAGLIFLOZIN; LINAGLIPTIN

Product Number

2

Dosage Form

-

Strength

25MG; 5MG

Approval Date

-

212364 / 2

Active Ingredient

EMPAGLIFLOZIN;LINAGLIPTIN

Application Number

212364

Product Number

2

Dosage Form

-

Strength

25MG; 5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 215139

Drug Name

GLYCEROL PHENYLBUTYRATE

Product Number

1

Dosage Form

-

Strength

1.1G/ML

Approval Date

-

215139 / 1

Active Ingredient

GLYCEROL PHENYLBUTYRATE

Application Number

215139

Product Number

1

Dosage Form

-

Strength

1.1G/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 218419

Drug Name

LISINOPRIL

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

-

218419 / 1

Active Ingredient

LISINOPRIL

Application Number

218419

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

-

Regulatory Status

Unclassified

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
    120 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
10 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

BRIVARACETAM

Application Number

214831

Product Number

2

Active Ingredient

BRIVARACETAM

Dosage Form

-

Strength

25mg

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