Breckenridge Pharmaceutical RX
FDA Approved Drugs

Breckenridge Pharmaceutical RX

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 7
  • Latest Approval Date Dec 06, 2011
  • Data Source FDA
  • First Approval Date Jan 11, 2008
All
9
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Discontinued
2
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RX
7
View
Company Overview

Company

Breckenridge Pharmaceutical RX

Country

U.S.A

Email

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Company Snapshot

Breckenridge Pharmaceutical RX

15 Massirio Drive, Suite 201 Berlin, CT 06037

U.S.A

www.bpirx.com/ View on Map
FDA Approved Drug Records ( 7 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

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Drug Status Breakdown
7 total
  • 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

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

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