Details for New Drug Application (NDA): 079112
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The generic ingredient in FEXOFENADINE HYDROCHLORIDE HIVES is fexofenadine hydrochloride. There are twenty-three drug master file entries for this compound. One hundred and four suppliers are listed for this compound. Additional details are available on the fexofenadine hydrochloride profile page.
Summary for 079112
Tradename: | FEXOFENADINE HYDROCHLORIDE HIVES |
Applicant: | Wockhardt |
Ingredient: | fexofenadine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 079112
Mechanism of Action | Histamine H1 Receptor Antagonists |
Suppliers and Packaging for NDA: 079112
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY | fexofenadine hydrochloride | TABLET;ORAL | 079112 | ANDA | TARGET Corporation | 11673-104 | 11673-104-12 | 1 BOTTLE, PLASTIC in 1 BOX (11673-104-12) / 120 TABLET, COATED in 1 BOTTLE, PLASTIC |
CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY | fexofenadine hydrochloride | TABLET;ORAL | 079112 | ANDA | TARGET Corporation | 11673-104 | 11673-104-15 | 1 BLISTER PACK in 1 CARTON (11673-104-15) / 15 TABLET, COATED in 1 BLISTER PACK |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 30MG | ||||
Approval Date: | Feb 8, 2012 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 30MG | ||||
Approval Date: | Feb 8, 2012 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 60MG | ||||
Approval Date: | Feb 8, 2012 | TE: | RLD: | No |
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