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NDC 50090-1234-00 Allegra Allergy 180 mg/1 Details
Allegra Allergy 180 mg/1
Allegra Allergy is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is FEXOFENADINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Fexofenadine is used to relieve the allergy symptoms of seasonal allergic rhinitis (''hay fever''), including runny nose; sneezing; red, itchy, or watery eyes; or itching of the nose, throat, or roof of the mouth in adults and children 2 years of age and older. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash in adults and children 6 months of age and older. Fexofenadine is in a class of medications called antihistamines. It works by blocking the effects of histamine, a substance in the body that causes allergy symptoms.
Related Packages: 50090-1234-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Fexofenadine
Product Information
| NDC | 50090-1234 |
|---|---|
| Product ID | 50090-1234_0f9c52c4-60a5-4054-885c-74e5eabc250a |
| Associated GPIs | 41550024100350 |
| GCN Sequence Number | 033716 |
| GCN Sequence Number Description | fexofenadine HCl TABLET 180 MG ORAL |
| HIC3 | Z2Q |
| HIC3 Description | ANTIHISTAMINES - 2ND GENERATION |
| GCN | 46594 |
| HICL Sequence Number | 011595 |
| HICL Sequence Number Description | FEXOFENADINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Allegra Allergy |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | fexofenadine hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 180 |
| Active Ingredient Units | mg/1 |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA020872 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-1234-00 (50090123400)
| NDC Package Code | 50090-1234-0 |
|---|---|
| Billing NDC | 50090123400 |
| Package | 1 BOTTLE, PLASTIC in 1 CARTON (50090-1234-0) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| Marketing Start Date | 2014-11-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |