Orchid Pharma
FDA Approved Drugs

Orchid Pharma

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 5
  • Latest Approval Date Feb 22, 2024
  • Data Source FDA
  • First Approval Date Dec 19, 2005
Company Overview

Company

Orchid Pharma

Country

India

Website

Visit Website

Email

corporate@orchidpharma.com

Social Profiles

Company Snapshot

Orchid Pharma

Orchid Towers’ 313, Valluvar Kottam High Road, Nungambakkam, Chennai - 600 034

India

www.orchidpharma.com/ corporate@orchidpharma.com View on Map
FDA Approved Drug Records ( 5 records )
2005
19 Dec
Discontinued Application: 65267

Drug Name

CEFPROZIL

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2005-12-19

65267 / 1

Active Ingredient

CEFPROZIL

Application Number

65267

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2005-12-19

Regulatory Status

Discontinued

2005
19 Dec
Discontinued Application: 65267

Drug Name

CEFPROZIL

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2005-12-19

65267 / 2

Active Ingredient

CEFPROZIL

Application Number

65267

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2005-12-19

Regulatory Status

Discontinued

2005
30 Dec
Discontinued Application: 65284

Drug Name

CEFPROZIL

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

2005-12-30

65284 / 1

Active Ingredient

CEFPROZIL

Application Number

65284

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

2005-12-30

Regulatory Status

Discontinued

2005
30 Dec
Discontinued Application: 65284

Drug Name

CEFPROZIL

Product Number

2

Dosage Form

-

Strength

125MG/5ML

Approval Date

2005-12-30

65284 / 2

Active Ingredient

CEFPROZIL

Application Number

65284

Product Number

2

Dosage Form

-

Strength

125MG/5ML

Approval Date

2005-12-30

Regulatory Status

Discontinued

2024
22 Feb
Discontinued Application: 216165

Drug Name

EXBLIFEP

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/VIAL;0.5GM/VIAL

Approval Date

2024-02-22

216165 / 1

Active Ingredient

CEFEPIME HYDROCHLORIDE; ENMETAZOBACTAM

Application Number

216165

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/VIAL;0.5GM/VIAL

Approval Date

2024-02-22

Regulatory Status

Discontinued

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Drug Status Breakdown
5 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

CEFPROZIL

Application Number

65267

Product Number

1

Active Ingredient

CEFPROZIL

Dosage Form

-

Strength

250MG

FDA Approved Drug Data

Approved drug product information

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