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NDC 72789-0196-10 Fexofenadine HCL 180 mg/1 Details
Fexofenadine HCL 180 mg/1
Fexofenadine HCL is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, 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: 72789-0196-10Last Updated: 05/19/2024
MedLinePlus Full Drug Details: Fexofenadine
Product Information
| NDC | 72789-0196 |
|---|---|
| Product ID | 72789-196_f6e158c9-9d02-13e9-e053-6394a90a1843 |
| 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 | Fexofenadine HCL |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Fexofenadine HCL |
| 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 | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA204097 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 72789-0196-10 (72789019610)
| NDC Package Code | 72789-196-10 |
|---|---|
| Billing NDC | 72789019610 |
| Package | 10 TABLET in 1 BOTTLE, PLASTIC (72789-196-10) |
| Marketing Start Date | 2023-03-14 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |