Pangea Biomed
FDA Approved Drugs

Pangea Biomed

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 RX
  • Total Records 9
  • Latest Approval Date Dec 09, 2020
  • Data Source FDA
  • First Approval Date Feb 24, 1983
All
9
View
Discontinued
4
View
RX
5
View
Company Overview

Company

Pangea Biomed

Country

Israel

Social Profiles

LinkedIn
Company Snapshot

Pangea Biomed

2A HaBarzel St. Tel Aviv

Israel

pangeabiomed.com/ info@pangeabiomed.com View on Map
FDA Approved Drug Records ( 9 records )
2020
09 Dec
Discontinued Application: 212925

Drug Name

CELECOXIB

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2020-12-09

212925 / 1

Active Ingredient

CELECOXIB

Application Number

212925

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2020-12-09

Regulatory Status

Discontinued

2020
09 Dec
Discontinued Application: 212925

Drug Name

CELECOXIB

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2020-12-09

212925 / 2

Active Ingredient

CELECOXIB

Application Number

212925

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2020-12-09

Regulatory Status

Discontinued

1983
28 Apr
RX Application: 88149

Drug Name

DEXAMETHASONE

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

1983-04-28

88149 / 1

Active Ingredient

DEXAMETHASONE

Application Number

88149

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

1983-04-28

Regulatory Status

RX

1983
24 Feb
RX Application: 87693

Drug Name

ERGOMAR

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1983-02-24

87693 / 1

Active Ingredient

ERGOTAMINE TARTRATE

Application Number

87693

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1983-02-24

Regulatory Status

RX

1997
11 Apr
RX Application: 74903

Drug Name

ETODOLAC

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1997-04-11

74903 / 1

Active Ingredient

ETODOLAC

Application Number

74903

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1997-04-11

Regulatory Status

RX

1999
19 Apr
RX Application: 74903

Drug Name

ETODOLAC

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1999-04-19

74903 / 2

Active Ingredient

ETODOLAC

Application Number

74903

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1999-04-19

Regulatory Status

RX

2001
31 Jan
RX Application: 75845

Drug Name

OXAPROZIN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2001-01-31

75845 / 1

Active Ingredient

OXAPROZIN

Application Number

75845

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2001-01-31

Regulatory Status

RX

1995
23 Jun
Discontinued Application: 74374

Drug Name

PRIMSOL

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/5ML

Approval Date

1995-06-23

74374 / 1

Active Ingredient

TRIMETHOPRIM HYDROCHLORIDE

Application Number

74374

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/5ML

Approval Date

1995-06-23

Regulatory Status

Discontinued

2000
24 Jan
Discontinued Application: 74973

Drug Name

PRIMSOL

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/5ML

Approval Date

2000-01-24

74973 / 1

Active Ingredient

TRIMETHOPRIM HYDROCHLORIDE

Application Number

74973

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/5ML

Approval Date

2000-01-24

Regulatory Status

Discontinued

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Drug Status Breakdown
9 total
  • Discontinued
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

CELECOXIB

Application Number

212925

Product Number

1

Active Ingredient

CELECOXIB

Dosage Form

-

Strength

200MG

FDA Approved Drug Data

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