Breckenridge Pharmaceutical
FDA Approved Drugs

Breckenridge Pharmaceutical

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 Discontinued
  • Total Records 9
  • Latest Approval Date Dec 06, 2011
  • Data Source FDA
  • First Approval Date May 26, 2006
All
9
View
Discontinued
2
View
RX
7
View
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Company

Breckenridge Pharmaceutical

Country

U.S.A

Website

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Company Snapshot

Breckenridge Pharmaceutical

15 Massirio Drive, Suite 201 Berlin, CT 06037

U.S.A

www.bpirx.com/ View on Map
FDA Approved Drug Records ( 9 records )
2008
17 Apr
RX Application: 78324

Drug Name

ESTRADIOL AND NORETHINDRONE ACETATE

Product Number

1

Dosage Form

-

Strength

1MG;0.5MG

Approval Date

2008-04-17

78324 / 1

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Application Number

78324

Product Number

1

Dosage Form

-

Strength

1MG;0.5MG

Approval Date

2008-04-17

Regulatory Status

RX

2011
09 Jun
RX Application: 78324

Drug Name

ESTRADIOL AND NORETHINDRONE ACETATE

Product Number

2

Dosage Form

-

Strength

0.5MG;0.1MG

Approval Date

2011-06-09

78324 / 2

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Application Number

78324

Product Number

2

Dosage Form

-

Strength

0.5MG;0.1MG

Approval Date

2011-06-09

Regulatory Status

RX

2011
06 Dec
RX Application: 40642

Drug Name

METHSCOPOLAMINE BROMIDE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2011-12-06

40642 / 1

Active Ingredient

METHSCOPOLAMINE BROMIDE

Application Number

40642

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2011-12-06

Regulatory Status

RX

2011
06 Dec
RX Application: 40642

Drug Name

METHSCOPOLAMINE BROMIDE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2011-12-06

40642 / 2

Active Ingredient

METHSCOPOLAMINE BROMIDE

Application Number

40642

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2011-12-06

Regulatory Status

RX

2008
11 Jan
RX Application: 78069

Drug Name

OXCARBAZEPINE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2008-01-11

78069 / 1

Active Ingredient

OXCARBAZEPINE

Application Number

78069

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2008-01-11

Regulatory Status

RX

2008
11 Jan
RX Application: 78069

Drug Name

OXCARBAZEPINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2008-01-11

78069 / 2

Active Ingredient

OXCARBAZEPINE

Application Number

78069

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2008-01-11

Regulatory Status

RX

2008
11 Jan
RX Application: 78069

Drug Name

OXCARBAZEPINE

Product Number

3

Dosage Form

-

Strength

600MG

Approval Date

2008-01-11

78069 / 3

Active Ingredient

OXCARBAZEPINE

Application Number

78069

Product Number

3

Dosage Form

-

Strength

600MG

Approval Date

2008-01-11

Regulatory Status

RX

2006
26 May
Discontinued Application: 77736

Drug Name

POLYETHYLENE GLYCOL 3350

Product Number

1

Dosage Form

-

Strength

17GM/SCOOPFUL

Approval Date

2006-05-26

77736 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350

Application Number

77736

Product Number

1

Dosage Form

-

Strength

17GM/SCOOPFUL

Approval Date

2006-05-26

Regulatory Status

Discontinued

2010
04 Jun
Discontinued Application: 77714

Drug Name

TERBINAFINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2010-06-04

77714 / 1

Active Ingredient

TERBINAFINE HYDROCHLORIDE

Application Number

77714

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2010-06-04

Regulatory Status

Discontinued

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Drug Status Breakdown
9 total
  • RX
  • 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

ESTRADIOL AND NORETHINDRONE ACETATE

Application Number

78324

Product Number

1

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Dosage Form

-

Strength

1MG;0.5MG

FDA Approved Drug Data

Approved drug product information

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