Carlsbad Technology, Inc.
FDA Approved Drugs

Carlsbad Technology, Inc.

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 Unclassified
  • Total Records 24
  • Latest Approval Date Jul 26, 2022
  • Data Source FDA
  • First Approval Date Nov 13, 1998
All
24
View
Unclassified
1
View
Discontinued
5
View
RX
18
View
Company Overview

Company

Carlsbad Technology, Inc.

Country

U.S.A

Website

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Company Snapshot

Carlsbad Technology, Inc.

CARLSBAD TECHNOLOGY, INC. 5922 Farnsworth Court Suite 102 Carlsbad CA 92008

U.S.A

www.carlsbadtechnologyinc.com/ View on Map
FDA Approved Drug Records ( 24 records )
1999
30 Apr
RX Application: 75382

Drug Name

ACYCLOVIR

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1999-04-30

75382 / 1

Active Ingredient

ACYCLOVIR

Application Number

75382

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1999-04-30

Regulatory Status

RX

1999
30 Apr
RX Application: 75382

Drug Name

ACYCLOVIR

Product Number

2

Dosage Form

-

Strength

800MG

Approval Date

1999-04-30

75382 / 2

Active Ingredient

ACYCLOVIR

Application Number

75382

Product Number

2

Dosage Form

-

Strength

800MG

Approval Date

1999-04-30

Regulatory Status

RX

2017
16 Aug
RX Application: 206261

Drug Name

ACYCLOVIR

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2017-08-16

206261 / 1

Active Ingredient

ACYCLOVIR

Application Number

206261

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2017-08-16

Regulatory Status

RX

2020
08 May
RX Application: 211068

Drug Name

AZITHROMYCIN

Product Number

1

Dosage Form

-

Strength

EQ 600MG BASE

Approval Date

2020-05-08

211068 / 1

Active Ingredient

AZITHROMYCIN

Application Number

211068

Product Number

1

Dosage Form

-

Strength

EQ 600MG BASE

Approval Date

2020-05-08

Regulatory Status

RX

2022
26 Jul
Discontinued Application: 211317

Drug Name

AZITHROMYCIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2022-07-26

211317 / 1

Active Ingredient

AZITHROMYCIN

Application Number

211317

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2022-07-26

Regulatory Status

Discontinued

-
Unclassified Application: 76126

Drug Name

CIPROFLOXACIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

76126 / 1

Active Ingredient

CIPROFLOXACIN

Application Number

76126

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

Regulatory Status

Unclassified

2004
09 Jun
RX Application: 76126

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

76126 / 2

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76126

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

Regulatory Status

RX

2004
09 Jun
RX Application: 76126

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

76126 / 3

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76126

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

Regulatory Status

RX

2004
09 Jun
RX Application: 76126

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

76126 / 4

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76126

Product Number

4

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

Regulatory Status

RX

1998
13 Nov
RX Application: 75185

Drug Name

DICLOFENAC SODIUM

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1998-11-13

75185 / 1

Active Ingredient

DICLOFENAC SODIUM

Application Number

75185

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

1998-11-13

Regulatory Status

RX

1998
13 Nov
RX Application: 75185

Drug Name

DICLOFENAC SODIUM

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1998-11-13

75185 / 2

Active Ingredient

DICLOFENAC SODIUM

Application Number

75185

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1998-11-13

Regulatory Status

RX

1998
13 Nov
RX Application: 75185

Drug Name

DICLOFENAC SODIUM

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1998-11-13

75185 / 3

Active Ingredient

DICLOFENAC SODIUM

Application Number

75185

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1998-11-13

Regulatory Status

RX

2020
13 Jul
Discontinued Application: 209680

Drug Name

ELETRIPTAN HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2020-07-13

209680 / 1

Active Ingredient

ELETRIPTAN HYDROBROMIDE

Application Number

209680

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2020-07-13

Regulatory Status

Discontinued

2020
13 Jul
Discontinued Application: 209680

Drug Name

ELETRIPTAN HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2020-07-13

209680 / 2

Active Ingredient

ELETRIPTAN HYDROBROMIDE

Application Number

209680

Product Number

2

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2020-07-13

Regulatory Status

Discontinued

2001
16 Apr
RX Application: 75805

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-16

75805 / 1

Active Ingredient

FAMOTIDINE

Application Number

75805

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-16

Regulatory Status

RX

2001
16 Apr
RX Application: 75805

Drug Name

FAMOTIDINE

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2001-04-16

75805 / 2

Active Ingredient

FAMOTIDINE

Application Number

75805

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2001-04-16

Regulatory Status

RX

2002
30 Jan
Discontinued Application: 76022

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-30

76022 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

76022

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-30

Regulatory Status

Discontinued

2002
30 Jan
Discontinued Application: 76022

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-30

76022 / 2

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

76022

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-30

Regulatory Status

Discontinued

2009
22 Sep
RX Application: 77911

Drug Name

GLIMEPIRIDE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2009-09-22

77911 / 1

Active Ingredient

GLIMEPIRIDE

Application Number

77911

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2009-09-22

Regulatory Status

RX

2009
22 Sep
RX Application: 77911

Drug Name

GLIMEPIRIDE

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2009-09-22

77911 / 2

Active Ingredient

GLIMEPIRIDE

Application Number

77911

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2009-09-22

Regulatory Status

RX

2009
22 Sep
RX Application: 77911

Drug Name

GLIMEPIRIDE

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

2009-09-22

77911 / 3

Active Ingredient

GLIMEPIRIDE

Application Number

77911

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

2009-09-22

Regulatory Status

RX

2002
05 Jun
RX Application: 75991

Drug Name

LOVASTATIN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2002-06-05

75991 / 1

Active Ingredient

LOVASTATIN

Application Number

75991

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2002-06-05

Regulatory Status

RX

2002
05 Jun
RX Application: 75991

Drug Name

LOVASTATIN

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2002-06-05

75991 / 2

Active Ingredient

LOVASTATIN

Application Number

75991

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2002-06-05

Regulatory Status

RX

2002
05 Jun
RX Application: 75991

Drug Name

LOVASTATIN

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

2002-06-05

75991 / 3

Active Ingredient

LOVASTATIN

Application Number

75991

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

2002-06-05

Regulatory Status

RX

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Drug Status Breakdown
24 total
  • RX
  • Discontinued
  • Unclassified
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

ACYCLOVIR

Application Number

75382

Product Number

1

Active Ingredient

ACYCLOVIR

Dosage Form

-

Strength

400MG

FDA Approved Drug Data

Approved drug product information

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