AbbVie Inc OTC
FDA Approved Drugs

AbbVie Inc OTC

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.

OTC
  • Total Records 2
  • Latest Approval Date Jan 25, 2013
  • Data Source FDA
  • First Approval Date Jul 28, 2010
All
301
View
Unclassified
19
View
Discontinued
158
View
OTC
2
View
RX
122
View
Company Overview

Company

AbbVie Inc OTC

Country

U.S.A

Social Profiles

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Company Snapshot

AbbVie Inc OTC

1 North Waukegan Road North Chicago, IL 60064

U.S.A

www.abbvie.com/ abbviecontractmfg@abbvie.com View on Map
FDA Approved Drug Records ( 2 records )
2010
28 Jul
OTC Application: 22134

Drug Name

LASTACAFT

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

2010-07-28

22134 / 1

Active Ingredient

ALCAFTADINE

Application Number

22134

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

2010-07-28

Regulatory Status

OTC

2013
25 Jan
OTC Application: 202211

Drug Name

OXYTROL FOR WOMEN

Product Number

1

Dosage Form

-

Strength

3.9MG/24HR

Approval Date

2013-01-25

202211 / 1

Active Ingredient

OXYBUTYNIN

Application Number

202211

Product Number

1

Dosage Form

-

Strength

3.9MG/24HR

Approval Date

2013-01-25

Regulatory Status

OTC

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Drug Status Breakdown
2 total
  • OTC
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

LASTACAFT

Application Number

22134

Product Number

1

Active Ingredient

ALCAFTADINE

Dosage Form

-

Strength

0.25%

FDA Approved Drug Data

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