Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations
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Search results from the "OB_OTC" table for query
on "020872."
| Active Ingredient: |
FEXOFENADINE HYDROCHLORIDE |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
CHILDREN'S ALLEGRA ALLERGY |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
30MG |
| Application Number: |
N020872 |
| Product Number: |
005 |
| Approval Date: |
Jan 24, 2011 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
OTC |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
FEXOFENADINE HYDROCHLORIDE |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
CHILDREN'S ALLEGRA HIVES |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
30MG |
| Application Number: |
N020872 |
| Product Number: |
006 |
| Approval Date: |
Jan 24, 2011 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
OTC |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
FEXOFENADINE HYDROCHLORIDE |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
ALLEGRA ALLERGY |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
60MG |
| Application Number: |
N020872 |
| Product Number: |
007 |
| Approval Date: |
Jan 24, 2011 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
OTC |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
FEXOFENADINE HYDROCHLORIDE |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
ALLEGRA HIVES |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
60MG |
| Application Number: |
N020872 |
| Product Number: |
008 |
| Approval Date: |
Jan 24, 2011 |
| Reference Listed Drug |
No |
| RX/OTC/DISCN: |
OTC |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
FEXOFENADINE HYDROCHLORIDE |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
ALLEGRA HIVES |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
180MG |
| Application Number: |
N020872 |
| Product Number: |
009 |
| Approval Date: |
Jan 24, 2011 |
| Reference Listed Drug |
Yes |
| RX/OTC/DISCN: |
OTC |
| Patent and Exclusivity Info for this product: |
View |
|
| Active Ingredient: |
FEXOFENADINE HYDROCHLORIDE |
| Dosage Form;Route: |
TABLET; ORAL |
| Proprietary Name: |
ALLEGRA ALLERGY |
| Applicant: |
SANOFI AVENTIS US |
| Strength: |
180MG |
| Application Number: |
N020872 |
| Product Number: |
010 |
| Approval Date: |
Jan 24, 2011 |
| Reference Listed Drug |
Yes |
| RX/OTC/DISCN: |
OTC |
| Patent and Exclusivity Info for this product: |
View |
|
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FDA/Center for Drug Evaluation and Research
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Office of Generic Drugs
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Division of Labeling and Program Support
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Update Frequency: |
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Orange Book Data - Monthly
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Generic Drug Product Information & Patent Information - Daily
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Orange Book Data Updated Through April, 2013
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Patent and Generic Drug Product Data Last Updated: May 21, 2013
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