Search by Drug Name or NDC
NDC 70000-0361-04 24HR Allergy Relief 180 mg/1 Details
24HR Allergy Relief 180 mg/1
24HR Allergy Relief is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by LEADER/ Cardinal Health 110, Inc.. 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: 70000-0361-04Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Fexofenadine
Product Information
| NDC | 70000-0361 |
|---|---|
| Product ID | 70000-0361_069eb55b-d2f0-1a2e-5ad8-ef68f7501c26 |
| 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 | 24HR Allergy Relief |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Fexofenadine hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 180 |
| Active Ingredient Units | mg/1 |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Labeler Name | LEADER/ Cardinal Health 110, Inc. |
| Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076502 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70000-0361-04 (70000036104)
| NDC Package Code | 70000-0361-4 |
|---|---|
| Billing NDC | 70000036104 |
| Package | 1 BOTTLE in 1 CARTON (70000-0361-4) / 90 TABLET in 1 BOTTLE |
| Marketing Start Date | 2018-04-27 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 0.25711 |
| Pricing Unit | EA |
| Effective Date | 2024-02-21 |
| NDC Description | ALLERGY RELIEF 180 MG TABLET |
| Pharmacy Type Indicator | C/I |
| OTC | Y |
| Explanation Code | 1 |
| Classification for Rate Setting | G |
| As of Date | 2024-02-21 |