Teyro Labs
FDA Approved Drugs

Teyro Labs

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.

RX
  • Total Records 9
  • Latest Approval Date Oct 23, 2023
  • Data Source FDA
  • First Approval Date Jan 18, 2007
Company Overview

Company

Teyro Labs

Country

India

Website

Visit Website

Email

info@teyro.com

Social Profiles

Company Snapshot

Teyro Labs

No.29, Thilak Street, T.Nagar, Chennai - 600017

India

www.teyro.com/our-group.html info@teyro.com View on Map
FDA Approved Drug Records ( 9 records )
2023
23 Oct
RX Application: 217237

Drug Name

CAPECITABINE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2023-10-23

217237 / 1

Active Ingredient

CAPECITABINE

Application Number

217237

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2023-10-23

Regulatory Status

RX

2023
23 Oct
RX Application: 217237

Drug Name

CAPECITABINE

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2023-10-23

217237 / 2

Active Ingredient

CAPECITABINE

Application Number

217237

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2023-10-23

Regulatory Status

RX

2007
18 Jan
RX Application: 77861

Drug Name

CARBOPLATIN

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2007-01-18

77861 / 1

Active Ingredient

CARBOPLATIN

Application Number

77861

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2007-01-18

Regulatory Status

RX

2007
18 Jan
RX Application: 77861

Drug Name

CARBOPLATIN

Product Number

2

Dosage Form

-

Strength

150MG/15ML (10MG/ML)

Approval Date

2007-01-18

77861 / 2

Active Ingredient

CARBOPLATIN

Application Number

77861

Product Number

2

Dosage Form

-

Strength

150MG/15ML (10MG/ML)

Approval Date

2007-01-18

Regulatory Status

RX

2007
18 Jan
RX Application: 77861

Drug Name

CARBOPLATIN

Product Number

3

Dosage Form

-

Strength

450MG/45ML (10MG/ML)

Approval Date

2007-01-18

77861 / 3

Active Ingredient

CARBOPLATIN

Application Number

77861

Product Number

3

Dosage Form

-

Strength

450MG/45ML (10MG/ML)

Approval Date

2007-01-18

Regulatory Status

RX

2007
18 Jan
RX Application: 77861

Drug Name

CARBOPLATIN

Product Number

4

Dosage Form

-

Strength

600MG/60ML (10MG/ML)

Approval Date

2007-01-18

77861 / 4

Active Ingredient

CARBOPLATIN

Application Number

77861

Product Number

4

Dosage Form

-

Strength

600MG/60ML (10MG/ML)

Approval Date

2007-01-18

Regulatory Status

RX

2011
25 Jul
RX Application: 78759

Drug Name

GEMCITABINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/VIAL

Approval Date

2011-07-25

78759 / 1

Active Ingredient

GEMCITABINE HYDROCHLORIDE

Application Number

78759

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/VIAL

Approval Date

2011-07-25

Regulatory Status

RX

2011
25 Jul
RX Application: 78759

Drug Name

GEMCITABINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2011-07-25

78759 / 2

Active Ingredient

GEMCITABINE HYDROCHLORIDE

Application Number

78759

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2011-07-25

Regulatory Status

RX

2010
01 Dec
RX Application: 91199

Drug Name

TOPOTECAN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE/VIAL

Approval Date

2010-12-01

91199 / 1

Active Ingredient

TOPOTECAN HYDROCHLORIDE

Application Number

91199

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE/VIAL

Approval Date

2010-12-01

Regulatory Status

RX

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Drug Status Breakdown
9 total
  • RX
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

CAPECITABINE

Application Number

217237

Product Number

1

Active Ingredient

CAPECITABINE

Dosage Form

-

Strength

150MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

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