Details for New Drug Application (NDA): 211075
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The generic ingredient in FEXOFENADINE HYDROCHLORIDE ALLERGY is fexofenadine hydrochloride. There are twenty-three drug master file entries for this compound. One hundred and one suppliers are listed for this compound. Additional details are available on the fexofenadine hydrochloride profile page.
Summary for 211075
Tradename: | FEXOFENADINE HYDROCHLORIDE ALLERGY |
Applicant: | Granules |
Ingredient: | fexofenadine hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 211075
Mechanism of Action | Histamine H1 Receptor Antagonists |
Suppliers and Packaging for NDA: 211075
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
FEXOFENADINE HYDROCHLORIDE ALLERGY | fexofenadine hydrochloride | TABLET;ORAL | 211075 | ANDA | Walgreens | 0363-8010 | 0363-8010-05 | 5 BLISTER PACK in 1 CARTON (0363-8010-05) / 1 TABLET, COATED in 1 BLISTER PACK |
FEXOFENADINE HYDROCHLORIDE ALLERGY | fexofenadine hydrochloride | TABLET;ORAL | 211075 | ANDA | Walgreens | 0363-8010 | 0363-8010-15 | 15 BLISTER PACK in 1 CARTON (0363-8010-15) / 1 TABLET, COATED in 1 BLISTER PACK |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 60MG | ||||
Approval Date: | Oct 18, 2019 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 180MG | ||||
Approval Date: | Oct 18, 2019 | TE: | RLD: | No |
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